Alphabetic Index | Tabular List | Neoplasms | Drugs and Chemicals | Injuries
Scarabiasis
B88.2
Scarlatina
(anginosa) (maligna)
A38.9
myocarditis
(acute)
A38.1
old
Myocarditis
otitis media
A38.0
ulcerosa
A38.8
Scarlet fever
(albuminuria) (angina)
A38.9
Schamberg's disease
(progressive pigmentary dermatosis)
L81.7
Schatzki's ring
(acquired) (esophagus) (lower)
K22.2
congenital
Q39.3
Schaufenster krankheit
I20.8
Schaumann's
benign lymphogranulomatosis
D86.1
disease or syndrome
Sarcoidosis
Scheie's syndrome
E76.03
Schenck's disease
B42.1
Scheuermann's disease or osteochondrosis
Osteochondrosis, juvenile, spine
Schilder disease
(-Flatau)
G37.0
Schilling-type monocytic leukemia
C93.0-
Schimmelbusch's disease, cystic mastitis, or hyperplasia
Mastopathy, cystic
Schistosoma infestation
Infestation, Schistosoma
Schistosomiasis
B65.9
with muscle disorder
B65.9
M63.80
ankle
B65.9
M63.87-
foot
B65.9
M63.87-
forearm
B65.9
M63.83-
hand
B65.9
M63.84-
lower leg
B65.9
M63.86-
multiple sites
B65.9
M63.89
pelvic region
B65.9
M63.85-
shoulder region
B65.9
M63.81-
specified site NEC
B65.9
M63.88
thigh
B65.9
M63.85-
upper arm
B65.9
M63.82-
Asiatic
B65.2
bladder
B65.0
chestermani
B65.8
colon
B65.1
cutaneous
B65.3
due to
S. haematobium
B65.0
S. japonicum
B65.2
S. mansoni
B65.1
S. mattheii
B65.8
Eastern
B65.2
genitourinary tract
B65.0
intestinal
B65.1
lung NEC
B65.9
J99
pneumonia
B65.9
J17
Manson's
(intestinal)
B65.1
oriental
B65.2
pulmonary NEC
B65.9
J99
pneumonia
B65.9
Schistosoma
haematobium
B65.0
japonicum
B65.2
mansoni
B65.1
specified type NEC
B65.8
urinary
B65.0
vesical
B65.0
Schizencephaly
Q04.6
Schizoaffective psychosis
F25.9
Schizodontia
K00.2
Schizoid personality
F60.1
Schizophrenia, schizophrenic
F20.9
acute
(brief) (undifferentiated)
F23
atypical
(form)
F20.3
borderline
F21
catalepsy
F20.2
catatonic
(type) (excited) (withdrawn)
F20.2
cenesthopathic, cenesthesiopathic
F20.89
childhood type
F84.5
chronic undifferentiated
F20.5
cyclic
F25.0
disorganized
(type)
F20.1
flexibilitas cerea
F20.2
hebephrenic
(type)
F20.1
incipient
F21
latent
F21
negative type
F20.5
paranoid
(type)
F20.0
paraphrenic
F20.0
post-psychotic depression
F32.89
prepsychotic
F21
prodromal
F21
pseudoneurotic
F21
pseudopsychopathic
F21
reaction
F23
residual
(state) (type)
F20.5
restzustand
F20.5
schizoaffective
(type)
Psychosis, schizoaffective
simple
(type)
F20.89
simplex
F20.89
specified type NEC
F20.89
spectrum and other psychotic disorder
F29
specified NEC
F28
stupor
F20.2
syndrome of childhood
F84.5
undifferentiated
(type)
F20.3
chronic
F20.5
Schizothymia
(persistent)
F60.1
Schlatter-Osgood disease or osteochondrosis
Osteochondrosis, juvenile, tibia
Schlatter's tibia
Osteochondrosis, juvenile, tibia
Schmidt's syndrome
(polyglandular, autoimmune)
E31.0
Schmincke's carcinoma or tumor
Neoplasm, nasopharynx, malignant
Schmitz dysentery
(-Stutzer)
A03.0
Schmorl's disease or nodes
lumbar region
M51.46
lumbosacral region
M51.47
sacrococcygeal region
M53.3
thoracic region
M51.44
thoracolumbar region
M51.45
Schneiderian
papilloma
Neoplasm, nasopharynx, benign
specified site
Neoplasm, benign, by site
unspecified site
D14.0
specified site
Neoplasm, malignant, by site
unspecified site
C30.0
Scholte's syndrome
(malignant carcinoid)
E34.0
Scholz disease or syndrome
(-Bielchowsky-Henneberg)
E75.25
Schönlein
(-Henoch) disease or purpura (primary) (rheumatic)
D69.0
Schottmuller's disease
A01.4
Schroeder's syndrome
(endocrine hypertensive)
E27.0
Schüller-Christian disease or syndrome
C96.5
Schultze's type acroparesthesia, simple
I73.89
Schultz's disease or syndrome
Agranulocytosis
Schwalbe-Ziehen-Oppenheim disease
G24.1
Schwannoma
Neoplasm, nerve, benign
malignant
Neoplasm, nerve, malignant
with rhabdomyoblastic differentiation
Neoplasm, nerve, malignant
melanocytic
Neoplasm, nerve, benign
pigmented
Neoplasm, nerve, benign
Schwannomatosis
Q85.03
Schwartz syndrome
(-Jampel)
G71.13
Schwartz-Bartter syndrome
E22.2
Schweniger-Buzzi anetoderma
L90.1
Sciatic
condition
Sciatica
(infective)
with lumbago
M54.4-
due to intervertebral disc disorder
Disorder, disc, with, radiculopathy
due to displacement of intervertebral disc
(with lumbago)
Disorder, disc, with, radiculopathy
wallet
M54.3-
Scimitar syndrome
Q26.8
Sclera
condition
Sclerectasia
H15.84-
Scleredema
adultorum
Sclerosis, systemic
Buschke's
Sclerosis, systemic
newborn
P83.0
Sclerema
(adiposum) (edematosum) (neonatorum) (newborn)
P83.0
adultorum
Sclerosis, systemic
Scleriasis
Scleroderma
Scleritis
H15.00-
with corneal involvement
H15.04-
anterior
H15.01-
brawny
H15.02-
in zoster
(due to)
B02.34
posterior
H15.03-
specified type NEC
H15.09-
syphilitic
A52.71
tuberculous
(nodular)
A18.51
Sclerochoroiditis
H31.8
Scleroconjunctivitis
Scleritis
Sclerocystic ovary syndrome
E28.2
Sclerodactyly, sclerodactylia
L94.3
Scleroderma, sclerodermia
(acrosclerotic) (diffuse) (generalized) (progressive) (pulmonary)
M34.9-
Sclerosis, systemic
circumscribed
L94.0
linear
L94.1
localized
L94.0
newborn
P83.88
systemic
M34.9
Sclerokeratitis
H16.8
tuberculous
A18.52
Scleroma nasi
A48.8
Scleromalacia
(perforans)
H15.05-
Scleromyxedema
L98.5
Sclérose en plaques
G35
Sclerosis, sclerotic
adrenal
(gland)
E27.8
Alzheimer's
Disease, Alzheimer's
amyotrophic
(lateral)
G12.21
aorta, aortic
I70.0
valve
Endocarditis, aortic
artery, arterial, arteriolar, arteriovascular
Arteriosclerosis
ascending multiple
G35
brain
(generalized) (lobular)
G37.9
artery, arterial
I67.2
diffuse
G37.0
disseminated
G35
insular
G35
Krabbe's
E75.23
miliary
G35
multiple
G35
presenile
(Alzheimer's)
Disease, Alzheimer's, early onset
senile
(arteriosclerotic)
I67.2
stem, multiple
G35
tuberous
Q85.1
bulbar, multiple
G35
bundle of His
I44.39
cardiac
Disease, heart, ischemic, atherosclerotic
cardiorenal
Hypertension, cardiorenal
cardiovascular
Disease, cardiovascular
renal
Hypertension, cardiorenal
cerebellar
Sclerosis, brain
cerebral
Sclerosis, brain
cerebrospinal
(disseminated) (multiple)
G35
cerebrovascular
I67.2
choroid
Degeneration, choroid
combined
(spinal cord)
Degeneration, combined
multiple
G35
concentric
(Balo)
G37.5
cornea
Opacity, cornea
coronary
(artery)
I25.10
with angina pectoris
Arteriosclerosis, coronary (artery),
corpus cavernosum
female
N90.89
male
N48.6
diffuse
(brain) (spinal cord)
G37.0
disseminated
G35
dorsal
G35
dorsolateral
(spinal cord)
Degeneration, combined
endometrium
N85.5
extrapyramidal
G25.9
eye, nuclear
(senile)
Cataract, senile, nuclear
focal and segmental
(glomerular)
N05.1
N00-N07 with fourth character .1
Friedreich's
(spinal cord)
G11.1
funicular
(spermatic cord)
N50.89
general
(vascular)
Arteriosclerosis
gland
(lymphatic)
I89.8
hepatic
K74.1
alcoholic
K70.2
hereditary
cerebellar
G11.9
spinal
(Friedreich's ataxia)
G11.1
hippocampal
G93.81
insular
G35
kidney
Sclerosis, renal
larynx
J38.7
lateral
(amyotrophic) (descending) (spinal)
G12.21
primary
G12.23
lens, senile nuclear
Cataract, senile, nuclear
liver
K74.1
with fibrosis
K74.2
alcoholic
K70.2
alcoholic
K70.2
cardiac
K76.1
lung
Fibrosis, lung
mastoid
Mastoiditis, chronic
mesial temporal
G93.81
mitral
I05.8
Mönckeberg's
(medial)
Arteriosclerosis, extremities
multiple
(brain stem) (cerebral) (generalized) (spinal cord)
G35
myocardium, myocardial
Disease, heart, ischemic, atherosclerotic
nuclear, eye
(senile)
Cataract, senile, nuclear
ovary
N83.8
pancreas
K86.89
penis
N48.6
peripheral arteries
Arteriosclerosis, extremities
plaques
G35
pluriglandular
E31.8
polyglandular
E31.8
posterolateral
(spinal cord)
Degeneration, combined
presenile
(Alzheimer's)
Disease, Alzheimer's, early onset
primary, lateral
G12.23
progressive, systemic
M34.0
pulmonary
Fibrosis, lung
artery
I27.0
valve
(heart)
Endocarditis, pulmonary
renal
N26.9
with
cystine storage disease
E72.09
hypertensive heart disease
(conditions in I11)
Hypertension, cardiorenal
arteriolar
(hyaline) (hyperplastic)
Hypertension, kidney
retina
(senile) (vascular)
H35.00
senile
(vascular)
Arteriosclerosis
spinal
(cord) (progressive)
G95.89
ascending
G61.0
combined
Degeneration, combined
multiple
G35
syphilitic
A52.11
disseminated
G35
dorsolateral
Degeneration, combined
hereditary
(Friedreich's) (mixed form)
G11.1
lateral
(amyotrophic)
G12.23
multiple
G35
posterior
(syphilitic)
A52.11
stomach
K31.89
subendocardial, congenital
I42.4
systemic
M34.9
with
lung involvement
M34.81
myopathy
M34.82
polyneuropathy
M34.83
drug-induced
M34.2
due to chemicals NEC
M34.2
progressive
M34.0
specified NEC
M34.89
temporal
(mesial)
G93.81
tricuspid
(heart) (valve)
I07.8
tuberous
(brain)
Q85.1
tympanic membrane
Disorder, tympanic membrane, specified NEC
valve, valvular
(heart)
Endocarditis
vascular
Arteriosclerosis
vein
I87.8
Scoliosis
(acquired) (postural)
M41.9
adolescent
(idiopathic)
Scoliosis, idiopathic, adolescent
congenital
Q67.5
due to bony malformation
Q76.3
failure of segmentation
(hemivertebra)
Q76.3
hemivertebra fusion
Q76.3
postural
Q67.5
idiopathic
M41.20
adolescent
M41.129
cervical region
M41.122
cervicothoracic region
M41.123
lumbar region
M41.126
lumbosacral region
M41.127
thoracic region
M41.124
thoracolumbar region
M41.125
cervical region
M41.22
cervicothoracic region
M41.23
infantile
M41.00
cervical region
M41.02
cervicothoracic region
M41.03
lumbar region
M41.06
lumbosacral region
M41.07
sacrococcygeal region
M41.08
thoracic region
M41.04
thoracolumbar region
M41.05
juvenile
M41.119
cervical region
M41.112
cervicothoracic region
M41.113
lumbar region
M41.116
lumbosacral region
M41.117
thoracic region
M41.114
thoracolumbar region
M41.115
lumbar region
M41.26
lumbosacral region
M41.27
thoracic region
M41.24
thoracolumbar region
M41.25
infantile
Scoliosis, idiopathic, infantile
neuromuscular
M41.40
cervical region
M41.42
cervicothoracic region
M41.43
lumbar region
M41.46
lumbosacral region
M41.47
occipito-atlanto-axial region
M41.41
thoracic region
M41.44
thoracolumbar region
M41.45
paralytic
Scoliosis, neuromuscular
postradiation therapy
M96.5
rachitic
(late effect or sequelae)
E64.3
M49.80
cervical region
E64.3
M49.82
cervicothoracic region
E64.3
M49.83
lumbar region
E64.3
M49.86
lumbosacral region
E64.3
M49.87
multiple sites
E64.3
M49.89
occipito-atlanto-axial region
E64.3
M49.81
sacrococcygeal region
E64.3
M49.88
thoracic region
E64.3
M49.84
thoracolumbar region
E64.3
M49.85
sciatic
M54.4-
secondary NEC
(to)
M41.50
cerebral palsy, Friedreich's ataxia, poliomyelitis, neuromuscular disorders
Scoliosis, neuromuscular
cervical region
M41.52
cervicothoracic region
M41.53
lumbar region
M41.56
lumbosacral region
M41.57
thoracic region
M41.54
thoracolumbar region
M41.55
specified form NEC
M41.80
cervical region
M41.82
cervicothoracic region
M41.83
lumbar region
M41.86
lumbosacral region
M41.87
thoracic region
M41.84
thoracolumbar region
M41.85
thoracogenic
M41.30
thoracic region
M41.34
thoracolumbar region
M41.35
tuberculous
A18.01
Scoliotic pelvis
with disproportion
(fetopelvic)
O33.0
causing obstructed labor
O65.0
Scorbutus, scorbutic
Scurvy
anemia
D53.2
Score, NIHSS
(National Institutes of Health Stroke Scale)
R29.7-
Scotoma
(arcuate) (Bjerrum) (central) (ring)
Defect, visual field, localized, scotoma
scintillating
H53.19
Scratch
Abrasion
Scratchy throat
R09.89
Screening
(for)
Z13.9
alcoholism
Z13.39
anemia
Z13.0
anomaly, congenital
Z13.89
antenatal, of mother
Z36.9
Encounter, antenatal screening
arterial hypertension
Z13.6
arthropod-borne viral disease NEC
Z11.59
autism
Z13.41
bacteriuria, asymptomatic
Z13.89
behavioral disorder
Z13.30
specified NEC
Z13.39
brain injury, traumatic
Z13.850
bronchitis, chronic
Z13.83
brucellosis
Z11.2
cardiovascular disorder
Z13.6
cataract
Z13.5
chlamydial diseases
Z11.8
cholera
Z11.0
chromosomal abnormalities NEC
(nonprocreative)
Z13.79
colonoscopy
Z12.11
congenital
dislocation of hip
Z13.89
eye disorder
Z13.5
malformation or deformation
Z13.89
contamination NEC
Z13.88
cystic fibrosis
Z13.228
dengue fever
Z11.59
dental disorder
Z13.84
depression
(adult) (adolescent) (child)
Z13.31
maternal
Z13.32
perinatal
Z13.32
developmental
delays
Z13.40
global
(milestones)
Z13.42
specified NEC
Z13.49
handicap
Z13.42
in early childhood
Z13.42
diabetes mellitus
Z13.1
diphtheria
Z11.2
disability, intellectual
Z13.39
disease or disorder
Z13.9
bacterial NEC
Z11.2
intestinal infectious
Z11.0
respiratory tuberculosis
Z11.1
behavioral
Z13.30
specified NEC
Z13.39
blood or blood-forming organ
Z13.0
cardiovascular
Z13.6
Chagas'
Z11.6
chlamydial
Z11.8
dental
Z13.89
developmental delays
Z13.40
global
(milestones)
Z13.42
specified NEC
Z13.49
digestive tract NEC
Z13.818
lower GI
Z13.811
upper GI
Z13.810
ear
Z13.5
endocrine
Z13.29
eye
Z13.5
genitourinary
Z13.89
heart
Z13.6
human immunodeficiency virus infection
(HIV)
Z11.4
immunity
Z13.0
infection
intestinal
Z11.0
specified NEC
Z11.6
infectious
Z11.9
mental health and behavioral
Z13.30
specified NEC
Z13.39
metabolic
Z13.228
neurological
Z13.89
nutritional
Z13.21
metabolic
Z13.228
lipoid disorders
Z13.220
protozoal
Z11.6
intestinal
Z11.0
respiratory
Z13.83
rheumatic
Z13.828
rickettsial
Z11.8
sexually-transmitted NEC
Z11.3
human immunodeficiency virus
(HIV)
Z11.4
sickle-cell
(trait)
Z13.0
skin
Z13.89
specified NEC
Z13.89
spirochetal
Z11.8
thyroid
Z13.29
vascular
Z13.6
venereal
Z11.3
viral NEC
Z11.59
human immunodeficiency virus
(HIV)
Z11.4
intestinal
Z11.0
elevated titer
Z13.89
emphysema
Z13.83
encephalitis, viral
(mosquito- or tick-borne)
Z11.59
exposure to contaminants
(toxic)
Z13.88
fever
dengue
Z11.59
hemorrhagic
Z11.59
yellow
Z11.59
filariasis
Z11.6
galactosemia
Z13.228
gastrointestinal condition
Z13.818
genetic - for procreative management
(nonprocreative)
Testing, genetic, for procreative management
disease carrier status
(nonprocreative)
Z13.71
specified NEC
(nonprocreative)
Z13.79
genitourinary condition
Z13.89
glaucoma
Z13.5
gonorrhea
Z11.3
gout
Z13.89
helminthiasis
(intestinal)
Z11.6
hematopoietic malignancy
Z12.89
hemoglobinopathies NEC
Z13.0
hemorrhagic fever
Z11.59
Hodgkin disease
Z12.89
human immunodeficiency virus
(HIV)
Z11.4
human papillomavirus
Z11.51
hypertension
Z13.6
immunity disorders
Z13.0
infant or child
(over 28 days old)
Z00.129
with abnormal findings
Z00.121
infection
mycotic
Z11.8
parasitic
Z11.8
ingestion of radioactive substance
Z13.88
intellectual disability
Z13.39
intestinal
helminthiasis
Z11.6
infectious disease
Z11.0
leishmaniasis
Z11.6
leprosy
Z11.2
leptospirosis
Z11.8
leukemia
Z12.89
lymphoma
Z12.89
malaria
Z11.6
malnutrition
Z13.29
metabolic
Z13.228
nutritional
Z13.21
measles
Z11.59
mental health disorder
Z13.30
specified NEC
Z13.39
metabolic errors, inborn
Z13.228
multiphasic
Z13.89
musculoskeletal disorder
Z13.828
osteoporosis
Z13.820
mycoses
Z11.8
myocardial infarction
(acute)
Z13.6
neoplasm
(malignant) (of)
Z12.9
bladder
Z12.6
blood
Z12.89
breast
Z12.39
routine mammogram
Z12.31
cervix
Z12.4
colon
Z12.11
genitourinary organs NEC
Z12.79
bladder
Z12.6
cervix
Z12.4
ovary
Z12.73
prostate
Z12.5
testis
Z12.71
vagina
Z12.72
hematopoietic system
Z12.89
intestinal tract
Z12.10
colon
Z12.11
rectum
Z12.12
small intestine
Z12.13
lung
Z12.2
lymph
(glands)
Z12.89
nervous system
Z12.82
oral cavity
Z12.81
prostate
Z12.5
rectum
Z12.12
respiratory organs
Z12.2
skin
Z12.83
small intestine
Z12.13
specified site NEC
Z12.89
stomach
Z12.0
nephropathy
Z13.89
nervous system disorders NEC
Z13.858
neurological condition
Z13.89
osteoporosis
Z13.820
parasitic infestation
Z11.9
specified NEC
Z11.8
phenylketonuria
Z13.228
plague
Z11.2
poisoning
(chemical) (heavy metal)
Z13.88
poliomyelitis
Z11.59
postnatal, chromosomal abnormalities
Z13.89
prenatal, of mother
Z36.9
Encounter, antenatal screening
protozoal disease
Z11.6
intestinal
Z11.0
pulmonary tuberculosis
Z11.1
radiation exposure
Z13.88
respiratory condition
Z13.83
respiratory tuberculosis
Z11.1
rheumatoid arthritis
Z13.828
rubella
Z11.59
schistosomiasis
Z11.6
sexually-transmitted disease NEC
Z11.3
human immunodeficiency virus
(HIV)
Z11.4
sickle-cell disease or trait
Z13.0
skin condition
Z13.89
sleeping sickness
Z11.6
special
Z13.9
specified NEC
Z13.89
syphilis
Z11.3
tetanus
Z11.2
trachoma
Z11.8
traumatic brain injury
Z13.850
trypanosomiasis
Z11.6
tuberculosis, respiratory
Z11.1
venereal disease
Z11.3
viral encephalitis
(mosquito- or tick-borne)
Z11.59
whooping cough
Z11.2
worms, intestinal
Z11.6
yaws
Z11.8
yellow fever
Z11.59
Scrofula, scrofulosis
(tuberculosis of cervical lymph glands)
A18.2
Scrofulide
(primary) (tuberculous)
A18.4
Scrofuloderma, scrofulodermia
(any site) (primary)
A18.4
Scrofulosus lichen
(primary) (tuberculous)
A18.4
Scrofulous
condition
Scrotal tongue
K14.5
Scrotum
condition
Scurvy, scorbutic
E54
anemia
D53.2
gum
E54
infantile
E54
rickets
E55.0
M90.80
Sealpox
B08.62
Seasickness
T75.3
Seatworm
(infection) (infestation)
B80
Sebaceous
condition
cyst
Cyst, sebaceous
Seborrhea, seborrheic
L21.9
capillitii
R23.8
capitis
L21.0
dermatitis
L21.9
infantile
L21.1
eczema
L21.9
infantile
L21.1
sicca
L21.0
Seckel's syndrome
Q87.1
Seclusion, pupil
Membrane, pupillary
Second hand tobacco smoke exposure
(acute) (chronic)
Z77.22
in the perinatal period
P96.81
Secondary
dentin
(in pulp)
K04.3
neoplasm, secondaries
Table of Neoplasms, secondary
Secretion
antidiuretic hormone, inappropriate
E22.2
catecholamine, by pheochromocytoma
E27.5
hormone
antidiuretic, inappropriate
(syndrome)
E22.2
by
carcinoid tumor
E34.0
pheochromocytoma
E27.5
ectopic NEC
E34.2
urinary
excessive
R35.8
suppression
R34
Section
nerve, traumatic
Injury, nerve
Sedative, hypnotic, or anxiolytic-induced
anxiety disorder
F13.980
bipolar and related disorder
F13.94
delirium
F13.921
depressive disorder
F13.94
major neurocognitive disorder
F13.97
mild neurocognitive disorder
F13.988
psychotic disorder
F13.959
sexual dysfunction
F13.981
sleep disorder
F13.982
Segmentation, incomplete
(congenital)
Fusion
bone NEC
Q78.8
lumbosacral
(joint) (vertebra)
Q76.49
Seitelberger's syndrome
(infantile neuraxonal dystrophy)
G31.89
Seizure
(s)
R56.9
Convulsions
akinetic
Epilepsy, generalized, specified NEC
atonic
Epilepsy, generalized, specified NEC
autonomic
(hysterical)
F44.5
convulsive
Convulsions
cortical
(focal) (motor)
Epilepsy, localization-related, symptomatic, with simple partial seizures
disorder
G40.909
Epilepsy
due to stroke
Sequelae (of), disease, cerebrovascular, by type, specified NEC
epileptic
Epilepsy
febrile
(simple)
R56.00
with status epilepticus
G40.901
complex
(atypical) (complicated)
R56.01
with status epilepticus
G40.901
grand mal
G40.409
intractable
G40.419
with status epilepticus
G40.411
without status epilepticus
G40.419
not intractable
G40.409
with status epilepticus
G40.401
without status epilepticus
G40.409
heart
Disease, heart
hysterical
F44.5
intractable
G40.919
with status epilepticus
G40.911
Jacksonian
(focal) (motor type) (sensory type)
Epilepsy, localization-related, symptomatic, with simple partial seizures
newborn
P90
nonspecific epileptic
atonic
Epilepsy, generalized, specified NEC
clonic
Epilepsy, generalized, specified NEC
myoclonic
Epilepsy, generalized, specified NEC
tonic
Epilepsy, generalized, specified NEC
tonic-clonic
Epilepsy, generalized, specified NEC
partial, developing into secondarily generalized seizures
complex
Epilepsy, localization-related, symptomatic, with complex partial seizures
simple
Epilepsy, localization-related, symptomatic, with simple partial seizures
petit mal
G40.409
intractable
G40.419
with status epilepticus
G40.411
without status epilepticus
G40.419
not intractable
G40.409
with status epilepticus
G40.401
without status epilepticus
G40.409
post traumatic
R56.1
recurrent
G40.909
specified NEC
G40.89
uncinate
Epilepsy, localization-related, symptomatic, with complex partial seizures
Selenium deficiency, dietary
E59
Self-damaging behavior
(life-style)
Z72.89
Self-harm
(attempted)
history
(personal)
Z91.5
in family
Z81.8
Self-mutilation
(attempted)
history
(personal)
Z91.5
in family
Z81.8
Self-poisoning
history
(personal)
Z91.5
in family
Z81.8
observation following attempt
(alleged)
Z03.6
Semicoma
R40.1
Seminal vesiculitis
N49.0
Seminoma
C62.9-
specified site
Neoplasm, malignant, by site
Senear-Usher disease or syndrome
L10.4
Senectus
R54
Senescence
(without mention of psychosis)
R54
Senile, senility
R41.81
condition
with
acute confusional state
F05
mental changes NOS
F03
psychosis NEC
Psychosis, senile
asthenia
R54
cervix
(atrophic)
N88.8
debility
R54
endometrium
(atrophic)
N85.8
fallopian tube
(atrophic)
Atrophy, fallopian tube
heart
(failure)
R54
ovary
(atrophic)
Atrophy, ovary
premature
E34.8
vagina, vaginitis
(atrophic)
N95.2
wart
L82.1
Sensation
burning
(skin)
R20.8
tongue
K14.6
loss of
R20.8
prickling
(skin)
R20.2
tingling
(skin)
R20.2
Sense loss
smell
Disturbance, sensation, smell
taste
Disturbance, sensation, taste
touch
R20.8
Sensibility disturbance
(cortical) (deep) (vibratory)
R20.9
Sensitive, sensitivity
Allergy
carotid sinus
G90.01
child
(excessive)
F93.8
cold, autoimmune
D59.1
dentin
K03.89
gluten
(non-celiac)
K90.41
latex
Z91.040
methemoglobin
D74.8
tuberculin, without clinical or radiological symptoms
R76.11
visual
glare
H53.71
impaired contrast
H53.72
Sensitiver Beziehungswahn
F22
Sensitization, auto-erythrocytic
D69.2
Separation
anxiety, abnormal
(of childhood)
F93.0
apophysis, traumatic - code as Fracture, by site
choroid
Detachment, choroid
epiphysis, epiphyseal
nontraumatic
Osteochondropathy, specified type NEC
upper femoral
Slipped, epiphysis, upper femoral
traumatic - code as Fracture, by site
fracture
Fracture
infundibulum cardiac from right ventricle by a partition
Q24.3
joint - code by site under Dislocation
(traumatic) (current)
pubic bone, obstetrical trauma
O71.6
retina, retinal
Detachment, retina
symphysis pubis, obstetrical trauma
O71.6
tracheal ring, incomplete, congenital
Q32.1
Sepsis
(generalized) (unspecified organism)
A41.9
with
organ dysfunction
(acute) (multiple)
R65.20
with septic shock
R65.21
actinomycotic
A42.7
adrenal hemorrhage syndrome
(meningococcal)
A39.1
anaerobic
A41.4
Bacillus anthracis
A22.7
Brucella
A23.9
Brucellosis
candidal
B37.7
cryptogenic
A41.9
due to device, implant or graft
T85.79
arterial graft NEC
T82.7
breast
(implant)
T85.79
catheter NEC
T85.79
dialysis
(renal)
T82.7
intraperitoneal
T85.71
infusion NEC
T82.7
spinal
(cranial) (epidural) (intrathecal) (spinal) (subarachnoid) (subdural)
T85.735
urethral indwelling
T83.511
urinary
T83.518
ectopic or molar pregnancy
O08.82
electronic
(electrode) (pulse generator) (stimulator)
bone
T84.7
cardiac
T82.7
nervous system
T85.738
brain
T85.731
neurostimulator generator
T85.734
peripheral nerve
T85.732
spinal cord
T85.733
urinary
T83.590
fixation, internal
(orthopedic)
Complication, fixation device, infection
gastrointestinal
(bile duct) (esophagus)
T85.79
neurostimulator electrode
(lead)
T85.732
genital
T83.69
heart NEC
T82.7
valve
(prosthesis)
T82.6
graft
T82.7
joint prosthesis
Complication, joint prosthesis, infection
ocular
(corneal graft) (orbital implant)
T85.79
orthopedic NEC
T84.7
fixation device, internal
Complication, fixation device, infection
specified NEC
T85.79
vascular
T82.7
ventricular intracranial shunt
(communicating)
T85.730
during labor
O75.3
Enterococcus
A41.81
Erysipelothrix
(rhusiopathiae) (erysipeloid)
A26.7
Escherichia coli
(E. coli)
A41.5
extraintestinal yersiniosis
A28.2
following
abortion
(subsequent episode)
O08.0
current episode
Abortion
ectopic or molar pregnancy
O08.82
immunization
T88.0
infusion, therapeutic injection or transfusion NEC
T80.29
obstetrical procedure
O86.04
gangrenous
A41.9
gonococcal
A54.86
Gram-negative
(organism)
A41.5
anaerobic
A41.4
Haemophilus influenzae
A41.3
herpesviral
B00.7
intra-abdominal
K65.1
intraocular
Endophthalmitis, purulent
Listeria monocytogenes
A32.7
localized - code to specific localized infection
in operation wound
T81.49
skin
Abscess
malleus
A24.0
melioidosis
A24.1
meningeal
Meningitis
meningococcal
A39.4
acute
A39.2
chronic
A39.3
MSSA
(Methicillin susceptible Staphylococcus aureus)
A41.01
newborn
P36.9
due to
anaerobes NEC
P36.5
Escherichia coli
P36.4
Staphylococcus
P36.30
aureus
P36.2
specified NEC
P36.39
Streptococcus
P36.10
group B
P36.0
specified NEC
P36.19
specified NEC
P36.8
Pasteurella multocida
A28.0
pelvic, puerperal, postpartum, childbirth
O85
postprocedural
T81.44
pneumococcal
A40.3
puerperal, postpartum, childbirth
(pelvic)
O85
Salmonella
(arizonae) (cholerae-suis) (enteritidis) (typhimurium)
A02.1
severe
R65.20
with septic shock
R65.21
skin, localized
Abscess
Shigella
A03.9
Dysentery, bacillary
specified organism NEC
A41.89
Staphylococcus, staphylococcal
A41.2
aureus
(methicillin susceptible) (MSSA)
A41.01
methicillin resistant
(MRSA)
A41.02
coagulase-negative
A41.1
specified NEC
A41.1
Streptococcus, streptococcal
A40.9
agalactiae
A40.1
group
A
A40.0
B
A40.1
D
A41.81
neonatal
P36.10
group B
P36.0
specified NEC
P36.19
pneumoniae
A40.3
pyogenes
A40.0
specified NEC
A40.8
tracheostomy stoma
J95.02
tularemic
A21.7
umbilical, umbilical cord
(newborn)
Sepsis, newborn
Yersinia pestis
A20.7
Septate
Septum
Septic
condition
arm
Cellulitis, upper limb
with lymphangitis
Lymphangitis, acute, upper limb
embolus
Embolism
finger
Cellulitis, digit
with lymphangitis
Lymphangitis, acute, digit
foot
Cellulitis, lower limb
with lymphangitis
Lymphangitis, acute, lower limb
gallbladder
(acute)
K81.0
hand
Cellulitis, upper limb
with lymphangitis
Lymphangitis, acute, upper limb
joint
Arthritis, pyogenic or pyemic
leg
Cellulitis, lower limb
with lymphangitis
Lymphangitis, acute, lower limb
nail
Cellulitis, digit
with lymphangitis
Lymphangitis, acute, digit
sore
Abscess
throat
J02.0
streptococcal
J02.0
spleen
(acute)
D73.89
teeth, tooth
(pulpal origin)
K04.4
throat
Pharyngitis
thrombus
Thrombosis
toe
Cellulitis, digit
with lymphangitis
Lymphangitis, acute, digit
tonsils, chronic
J35.01
with adenoiditis
J35.03
uterus
Endometritis
Septicemia
A41.9
meaning sepsis
Sepsis
Septum, septate
(congenital)
Anomaly, by site
anal
Q42.3
with fistula
Q42.2
aqueduct of Sylvius
Q03.0
with spina bifida
Spina bifida, by site, with hydrocephalus
uterus
Q51.20
complete
Q51.21
partial
Q51.22
specified NEC
Q51.28
vagina
Q52.10
in pregnancy
Pregnancy, complicated by, abnormal vagina
causing obstructed labor
O65.5
longitudinal
Q52.129
microperforate
left side
Q52.124
right side
Q52.123
nonobstruction
Q52.120
obstructing
Q52.129
left side
Q52.122
right side
Q52.121
transverse
Q52.11
Sequelae
(of)
condition
abscess, intracranial or intraspinal
(conditions in G06)
G09
amputation -- code to injury with seventh character S
burn and corrosion -- code to injury with seventh character S
calcium deficiency
E64.8
cerebrovascular disease
Sequelae, disease, cerebrovascular
childbirth
O94
contusion -- code to injury with seventh character S
corrosion
Sequelae, burn and corrosion
crushing injury -- code to injury with seventh character S
disease
cerebrovascular
I69.90
alteration of sensation
I69.998
aphasia
I69.920
apraxia
I69.990
ataxia
I69.993
cognitive deficits
I69.91
disturbance of vision
I69.998
dysarthria
I69.922
dysphagia
I69.991
dysphasia
I69.921
facial droop
I69.992
facial weakness
I69.992
fluency disorder
I69.923
hemiplegia
I69.95-
hemorrhage
intracerebral
Sequelae, hemorrhage, intracerebral
intracranial, nontraumatic NEC
Sequelae, hemorrhage, intracranial, nontraumatic
subarachnoid
Sequelae, hemorrhage, subarachnoid
language deficit
I69.928
monoplegia
lower limb
I69.94-
upper limb
I69.93-
paralytic syndrome
I69.96-
specified effect NEC
I69.998
specified type NEC
I69.80
alteration of sensation
I69.898
aphasia
I69.820
apraxia
I69.890
ataxia
I69.893
cognitive deficits
I69.81
disturbance of vision
I69.898
dysarthria
I69.822
dysphagia
I69.891
dysphasia
I69.821
facial droop
I69.892
facial weakness
I69.892
fluency disorder
I69.823
hemiplegia
I69.85-
language deficit
I69.828
monoplegia
lower limb
I69.84-
upper limb
I69.83-
paralytic syndrome
I69.86-
specified effect NEC
I69.898
speech deficit
I69.928
speech deficit
I69.828
stroke NOS
Sequelae, stroke NOS
dislocation -- code to injury with seventh character S
encephalitis or encephalomyelitis
(conditions in G04)
G09
in infectious disease NEC
B94.8
viral
B94.1
external cause -- code to injury with seventh character S
foreign body entering natural orifice -- code to injury with seventh character S
fracture -- code to injury with seventh character S
frostbite -- code to injury with seventh character S
Hansen's disease
B92
hemorrhage
intracerebral
I69.10
alteration of sensation
I69.198
aphasia
I69.120
apraxia
I69.190
ataxia
I69.193
cognitive deficits
I69.11
disturbance of vision
I69.198
dysarthria
I69.122
dysphagia
I69.191
dysphasia
I69.121
facial droop
I69.192
facial weakness
I69.192
fluency disorder
I69.123
hemiplegia
I69.15-
language deficit NEC
I69.128
monoplegia
lower limb
I69.14-
upper limb
I69.13-
paralytic syndrome
I69.16-
specified effect NEC
I69.198
speech deficit NEC
I69.128
intracranial, nontraumatic NEC
I69.20
alteration of sensation
I69.298
aphasia
I69.220
apraxia
I69.290
ataxia
I69.293
cognitive deficits
I69.21
disturbance of vision
I69.298
dysarthria
I69.222
dysphagia
I69.291
dysphasia
I69.221
facial droop
I69.292
facial weakness
I69.292
fluency disorder
I69.223
hemiplegia
I69.25-
language deficit NEC
I69.228
monoplegia
lower limb
I69.24-
upper limb
I69.23-
paralytic syndrome
I69.26-
specified effect NEC
I69.298
speech deficit NEC
I69.228
subarachnoid
I69.00
alteration of sensation
I69.098
aphasia
I69.020
apraxia
I69.090
ataxia
I69.093
cognitive deficits
I69.01-
disturbance of vision
I69.098
dysarthria
I69.022
dysphagia
I69.091
dysphasia
I69.021
facial droop
I69.092
facial weakness
I69.092
fluency disorder
I69.023
hemiplegia
I69.05-
language deficit NEC
I69.028
monoplegia
lower limb
I69.04-
upper limb
I69.03-
paralytic syndrome
I69.06-
specified effect NEC
I69.098
speech deficit NEC
I69.028
hepatitis, viral
B94.2
hyperalimentation
E68
infarction
cerebral
I69.30
alteration of sensation
I69.398
aphasia
I69.320
apraxia
I69.390
ataxia
I69.393
cognitive deficits
I69.31
disturbance of vision
I69.398
dysarthria
I69.322
dysphagia
I69.391
dysphasia
I69.321
facial droop
I69.392
facial weakness
I69.392
fluency disorder
I69.323
hemiplegia
I69.35-
language deficit NEC
I69.328
monoplegia
lower limb
I69.34-
upper limb
I69.33-
paralytic syndrome
I69.36-
specified effect NEC
I69.398
speech deficit NEC
I69.328
infection, pyogenic, intracranial or intraspinal
G09
infectious disease
B94.9
specified NEC
B94.8
injury -- code to injury with seventh character S
leprosy
B92
meningitis
bacterial
(conditions in G00)
G09
other or unspecified cause
(conditions in G03)
G09
muscle injury -- code to injury with seventh character S
(and tendon)
myelitis
Sequelae, encephalitis
niacin deficiency
E64.8
nutritional deficiency
E64.9
specified NEC
E64.8
obstetrical condition
O94
parasitic disease
B94.9
phlebitis or thrombophlebitis of intracranial or intraspinal venous sinuses and veins
(conditions in G08)
G09
poisoning -- code to poisoning with seventh character S
nonmedicinal substance
Sequelae, toxic effect, nonmedicinal substance
poliomyelitis
(acute)
B91
pregnancy
O94
protein-energy malnutrition
E64.0
puerperium
O94
rickets
E64.3
selenium deficiency
E64.8
sprain and strain -- code to injury with seventh character S
stroke NOS
I69.30
alteration in sensation
I69.398
aphasia
I69.320
apraxia
I69.390
ataxia
I69.393
cognitive deficits
I69.31
disturbance of vision
I69.398
dysarthria
I69.322
dysphagia
I69.391
dysphasia
I69.321
facial droop
I69.392
facial weakness
I69.392
hemiplegia
I69.35-
language deficit NEC
I69.328
monoplegia
lower limb
I69.34-
upper limb
I69.33-
paralytic syndrome
I69.36-
specified effect NEC
I69.398
speech deficit NEC
I69.328
tendon and muscle injury -- code to injury with seventh character S
thiamine deficiency
E64.8
trachoma
B94.0
tuberculosis
B90.9
bones and joints
B90.2
central nervous system
B90.0
genitourinary
B90.1
pulmonary
(respiratory)
B90.9
specified organs NEC
B90.8
viral
encephalitis
B94.1
hepatitis
B94.2
vitamin deficiency NEC
E64.8
A
E64.1
B
E64.8
C
E64.2
wound, open -- code to injury with seventh character S
Sequestration
Sequestrum
disk
Displacement, intervertebral disk
lung, congenital
Q33.2
Sequestrum
bone
Osteomyelitis, chronic
dental
M27.2
jaw bone
M27.2
orbit
Osteomyelitis, orbit
sinus
(accessory) (nasal)
Sinusitis
Sequoiosis lung or pneumonitis
J67.8
Serology for syphilis
doubtful
with signs or symptoms - code by site and stage under Syphilis
follow-up of latent syphilis
Syphilis, latent
negative, with signs or symptoms - code by site and stage under Syphilis
positive
A53.0
with signs or symptoms - code by site and stage under Syphilis
reactivated
A53.0
Seroma
Hematoma
postprocedural
Complication, postprocedural, seroma
traumatic, secondary and recurrent
T79.2
Seropurulent
condition
Serositis, multiple
K65.8
pericardial
I31.1
peritoneal
K65.8
Serous
condition
Sertoli cell
adenoma
specified site
Neoplasm, benign, by site
unspecified site
female
D27.9
male
D29.20
carcinoma
specified site
Neoplasm, malignant, by site
unspecified site
(male)
C62.9-
female
C56.9
tumor
with lipid storage
specified site
Neoplasm, benign, by site
unspecified site
female
D27.9
male
D29.20
specified site
Neoplasm, benign, by site
unspecified site
female
D27.9
male
D29.20