AMH
(asymptomatic microscopic hematuria)
R31.21
Amnes
(t)ic syndrome (post-traumatic)
F04
Amnionitis
Pregnancy, complicated by
Amputation
Absence, by site, acquired
neuroma
(postoperative) (traumatic)
Complications, amputation stump, neuroma
abnormal, painful, or with complication
(late)
Complications, amputation stump
traumatic
(complete) (partial)
arm
(upper) (complete)
S48.91-
shoulder joint
(complete)
S48.01-
elbow and wrist
(complete)
S58.11-
shoulder and elbow
(complete)
S48.11-
clitoris
(complete)
S38.211
finger
(complete) (metacarpophalangeal)
S68.11-
thumb
Amputation, traumatic, thumb
transphalangeal
(complete)
S68.61-
at elbow level
(complete)
S58.01-
between elbow and wrist
(complete)
S58.11-
genital organ
(s) (external)
hand
(complete) (wrist level)
S68.41-
finger alone
(s)
Amputation, traumatic, finger
thumb alone
Amputation, traumatic, thumb
transmetacarpal
(complete)
S68.71-
ear
Amputation, traumatic, ear
hip
(and thigh) (complete)
S78.91-
at hip joint
(complete)
S78.01-
between hip and knee
(complete)
S78.11-
labium
(majus) (minus) (complete)
S38.21-
between knee and ankle
S88.11-
shoulder
Amputation, traumatic, arm
at shoulder joint
Amputation, traumatic, arm, at shoulder joint
thigh
Amputation, traumatic, hip
breast
Amputation, traumatic, breast
thumb
(complete) (metacarpophalangeal)
S68.01-
transphalangeal
(complete)
S68.51-
Amyelencephalus, amyelencephaly
Q00.0
Amylopectinosis
(brancher enzyme deficiency)
E74.03
Amyotrophia, amyotrophy, amyotrophic
G71.8
diabetic
Diabetes, amyotrophy
Anaphylactoid shock or reaction
Shock, anaphylactic
Anaphylactoid syndrome of pregnancy
O88.01-
Ancylostoma, ancylostomiasis
(braziliense) (caninum) (ceylanicum) (duodenale)
B76.0
Androgen insensitivity syndrome
E34.50
Syndrome, androgen insensitivity
Androgen resistance syndrome
E34.50
Syndrome, androgen insensitivity
Anemia
(essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound)
D64.9
anaerobic glycolysis
D55.2
pentose phosphate pathway
D55.1
Addison
(-Biermer) (pernicious)
D51.0
agranulocytic
Agranulocytosis
amino-acid-deficiency
D53.0
Biermer's
(pernicious)
D51.0
bothriocephalus
B70.0
D63.8
chronica congenita aregenerativa
D61.09
combined system disease NEC
D51.0
G32.0
due to dietary vitamin B12 deficiency
D51.3
G32.0
complicating pregnancy, childbirth or puerperium
Pregnancy, complicated by (management affected by), anemia
due to isoimmunization NOS
P55.9
dyserythropoietic, dyshematopoietic
D64.4
following fetal blood loss
P61.3
hereditary hemolytic NOS
D58.9
Cooley's
(erythroblastic)
D56.1
2, 3 diphosphoglycurate mutase
D55.2
6 phosphogluconate dehydrogenase
D55.1
combined B12 and folate
D53.1
drug-induced
(hemolytic)
D59.2
glucose-6-phosphate dehydrogenase
(G6PD)
D55.0
nucleotide metabolism
D55.3
related to hexose monophosphate shunt pathway NEC
(HMP)
D55.1
erythrocytic glutathione
D55.1
glucose-6-phosphate dehydrogenase
D55.0
glutathione reductase
D55.1
glyceraldehyde phosphate dehydrogenase
D55.2
secondary to blood loss
(chronic)
D50.0
poor iron absorption
D50.8
specified deficiency NEC
D53.8
phosphofructo-aldolase
D55.2
phosphoglycerate kinase
D55.2
triose-phosphate isomerase
D55.2
intrinsic factor deficiency
D51.0
selective vitamin B12 malabsorption with proteinuria
D51.1
Diamond-Blackfan
(congenital hypoplastic)
D61.01
dibothriocephalus
B70.0
D63.8
Diphyllobothrium
(Dibothriocephalus)
B70.0
D63.8
antineoplastic chemotherapy
D64.81
chemotherapy, antineoplastic
D64.81
chronic disease classified elsewhere NEC
D63.8
chronic kidney disease
D63.1
dietary vitamin B12 deficiency
D51.3
glutathione metabolism
D55.1
nucleotide metabolism
D55.3
drug
Anemia, by type
Table of Drugs and Chemicals
end stage renal disease
D63.1
fish tapeworm infestation
(D.latum)
B70.0
D63.8
loss of blood
(chronic)
D50.0
Necator americanus
B76.1
D63.8
selective vitamin B12 malabsorption with proteinuria
D51.1
transcobalamin II deficiency
D51.2
Dyke-Young type
(secondary) (symptomatic)
D59.1
dyserythropoietic
(congenital)
D64.4
dyshematopoietic
(congenital)
D64.4
elliptocytosis
Elliptocytosis
enzyme-deficiency, drug-induced
D59.2
epidemic
B76.9
D63.8
Ancylostomiasis
newborn
P55.9
Disease, hemolytic
erythrocytic glutathione deficiency
D55.1
erythropoietin-resistant anemia
(EPO resistant anemia)
D63.1
Faber's
(achlorhydric anemia)
D50.9
factitious
(self-induced blood letting)
D50.0
familial erythroblastic
D56.1
Fanconi's
(congenital pancytopenia)
D61.09
fish tapeworm infestation
(D. latum)
B70.0
D63.8
folate deficiency
(folic acid)
D52.9
glucose-6-phosphate dehydrogenase deficiency
(G6PD)
D55.0
glutathione-reductase deficiency
D55.1
granulocytic
Agranulocytosis
Heinz body, congenital
D58.2
with hemoglobinuria NEC
D59.6
due to enzyme deficiency specified type NEC
D55.8
cold type
(secondary) (symptomatic)
D59.1
congenital
(spherocytic)
Spherocytosis
drugs
(nonautoimmune)
D59.2
presence of shunt or other internal prosthetic device
D59.4
due to enzyme disorder
D55.9
congenital or hereditary NEC
D55.8
glucose-6-phosphate dehydrogenase deficiency
D55.0
pyruvate kinase deficiency
D55.2
specified type NEC
(hereditary)
D58.8
Stransky-Regala type
D58.8
Hemoglobinopathy
warm type
(secondary) (symptomatic)
D59.1
hemorrhagic
(chronic)
D50.0
hexokinase deficiency
D55.2
hypochromic
(idiopathic) (microcytic) (normoblastic)
D50.9
due to blood loss
(chronic)
D50.0
pyridoxine-responsive
D64.3
sideroblastic, sex-linked
D64.0
hypoplasia, red blood cells
D61.9
congenital or familial
D61.01
hypoplastic
(idiopathic)
D61.9
congenital or familial
(of childhood)
D61.01
hypoproliferative
(refractive)
D61.9
chronic kidney disease
D63.1
end stage renal disease
D63.1
failure, kidney
(renal)
D63.1
neoplastic disease
D63.0
Neoplasm
intertropical
D63.8
Ancylostomiasis
secondary to blood loss
(chronic)
D50.0
Joseph-Diamond-Blackfan
(congenital hypoplastic)
D61.01
Lederer's
(hemolytic)
D59.1
leukoerythroblastic
D61.82
malignant
(progressive)
D51.0
Mediterranean
(with other hemoglobinopathy)
D56.9
combined B12 and folate deficiency
D53.1
microcytic
(hypochromic)
D50.9
due to blood loss
(chronic)
D50.0
microdrepanocytosis
D57.40
microelliptopoikilocytic
(Rietti-Greppi- Micheli)
D56.9
ABO
(antibodies, isoimmunization, maternal/fetal incompatibility)
P55.1
Rh
(antibodies, isoimmunization, maternal/fetal incompatibility)
P55.0
following fetal blood loss
P61.3
posthemorrhagic
(fetal)
P61.3
nonspherocytic hemolytic
Anemia, hemolytic, nonspherocytic
normocytic
(infectional)
D64.9
due to blood loss
(chronic)
D50.0
nutritional
(deficiency)
D53.9
poor iron absorption
D50.8
specified deficiency NEC
D53.8
orotaciduric
(congenital) (hereditary)
D53.0
ovalocytosis
(hereditary)
Elliptocytosis
pernicious
(congenital) (malignant) (progressive)
D51.0
posthemorrhagic
(chronic)
D50.0
postoperative
(postprocedural)
due to blood loss
(acute)
D62
pseudoleukemica infantum
D64.89
pyridoxine-responsive
D64.3
pyruvate kinase deficiency
D55.2
in transformation
(RAEB T)
Leukemia, acute myeloblastic
sideroblasts
(ring) (RARS)
D46.1
without ring sideroblasts, so stated
D46.0
without sideroblasts without excess of blasts
D46.0
Rietti-Greppi-Micheli
D56.9
sickle-cell
Disease, sickle-cell
hypochromic, sex-linked
D64.0
pyridoxine-responsive NEC
D64.3
sideropenic
(refractory)
D50.9
due to blood loss
(chronic)
D50.0
spherocytic
(hereditary)
Spherocytosis
syphilitic
(acquired) (late)
A52.79
D63.8
thrombocytopenic
Thrombocytopenia
B12 deficiency pernicious
(dietary)
D51.0
Witts'
(achlorhydric anemia)
D50.8
Anencephalus, anencephaly
Q00.0
Aneurysm
(anastomotic) (artery) (cirsoid) (diffuse) (false) (fusiform) (multiple) (saccular)
I72.9
aorta, aortic
(nonsyphilitic)
I71.9
thorax, thoracic
(arch)
I71.2
valve
(heart)
I35.8
Endocarditis, aortic
ruptured
Hemorrhage, intracranial, subarachnoid
arteriovenous
(congenital)
Malformation, arteriovenous
peripheral
Malformation, arteriovenous, peripheral
specified site NEC
Malformation, arteriovenous
berry
(congenital) (nonruptured)
I67.1
ruptured
Hemorrhage, intracranial, subarachnoid
arteriovenous
(congenital) (nonruptured)
Q28.2
berry
(congenital) (nonruptured)
I67.1
ruptured
I60.7
Hemorrhage, intracranial, subarachnoid
miliary
(congenital) (nonruptured)
I67.1
ruptured
I60.7
Hemorrhage, intracranial, subarachnoid
ruptured
Hemorrhage, intracranial, subarachnoid
syphilitic
(hemorrhage)
A52.05
cardiac
(false)
I25.3
Aneurysm, heart
carotid artery
(common) (external)
I72.0
internal
(intracranial)
I67.1
extracranial portion
I72.0
ruptured into brain
I60.0-
arteriovenous
(congenital) (nonruptured)
Q28.3
central nervous system, syphilitic
A52.05
congenital
(peripheral)
Q27.8
aorta
(root) (sinus)
Q25.43
conjunctiva
Abnormality, conjunctiva, vascular
conus arteriosus
Aneurysm, heart
coronary
(arteriosclerotic) (artery)
I25.41
arteriovenous, congenital
Q24.5
ruptured
Infarct, myocardium
endocardial, infective
(any valve)
I33.0
femoral
(artery) (ruptured)
I72.4
heart
(wall) (chronic or with a stated duration of over 4 weeks)
I25.3
iliac
(common) (artery) (ruptured)
I72.3
endocardial
(any valve)
I33.0
innominate
(nonsyphilitic)
I72.8
interauricular septum
Aneurysm, heart
interventricular septum
Aneurysm, heart
intrathoracic
(nonsyphilitic)
I71.2
lung
(pulmonary artery)
I28.1
mediastinal
(nonsyphilitic)
I72.8
ruptured
Hemorrhage, intracerebral, subarachnoid, intracranial
mitral
(heart) (valve)
I34.8
endocardial
(any valve)
I33.0
ruptured, brain
Hemorrhage, intracerebral, subarachnoid
myocardium
Aneurysm, heart
patent ductus arteriosus
Q25.0
popliteal
(artery) (ruptured)
I72.4
congenital
(nonruptured)
Q28.1
valve
(heart)
Endocarditis, pulmonary
racemose
(peripheral)
I72.9
congenital
Aneurysm, congenital
retina
Disorder, retina, microaneurysms
diabetic
Diabetes, microaneurysms, retinal
syphilitic
(hemorrhage)
A52.09
subclavian
(artery) (ruptured)
I72.8
central nervous system
A52.05
congenital
(late)
A50.54
I79.0
thoracoabdominal
(aorta)
I71.6
thorax, thoracic
(aorta) (arch) (nonsyphilitic)
I71.2
traumatic, specified site
(complication) (early)
Injury, blood vessel
tricuspid
(heart) (valve)
I07.8
upper limb
(ruptured)
I72.1
valve, valvular
Endocarditis
Angina
(attack) (cardiac) (chest) (heart) (pectoris) (syndrome) (vasomotor)
I20.9
atherosclerotic heart disease
Arteriosclerosis, coronary (artery),
accelerated
Angina, unstable
agranulocytic
Agranulocytosis
angiospastic
Angina, with documented spasm
crescendo
Angina, unstable
de novo effort
Angina, unstable
diphtheritic, membranous
A36.0
following acute myocardial infarction
I23.7
gangrenous diphtheritic
A36.0
malignant diphtheritic
A36.0
monocytic
Mononucleosis, infectious
of effort
Angina, specified NEC
pre-infarctional
Angina, unstable
Prinzmetal
Angina, with documented spasm
progressive
Angina, unstable
pultaceous, diphtheritic
A36.0
spasm-induced
Angina, with documented spasm
stenocardia
Angina, specified NEC
stridulous, diphtheritic
A36.2
variant
Angina, with documented spasm
worsening effort
Angina, unstable
Angioblastoma
Neoplasm, connective tissue, uncertain behavior
Angioedema
(allergic) (any site) (with urticaria)
T78.3
Angioendothelioma
Neoplasm, uncertain behavior, by site
bone
Neoplasm, bone, malignant
Ewing's
Neoplasm, bone, malignant
Angiofibroma
Neoplasm, benign, by site
specified site
Neoplasm, benign, by site
Angioid streaks
(choroid) (macula) (retina)
H35.33
Angioleiomyoma
Neoplasm, connective tissue, benign
Angiomyoliposarcoma
Neoplasm, connective tissue, malignant
Angiomyoma
Neoplasm, connective tissue, benign
Angiomyosarcoma
Neoplasm, connective tissue, malignant
Angiomyxoma
Neoplasm, connective tissue, uncertain behavior
Angioneurotic edema
(allergic) (any site) (with urticaria)
T78.3
Angiosarcoma
Neoplasm, connective tissue, malignant
Angiospasm
(peripheral) (traumatic) (vessel)
I73.9
arm
Mononeuropathy, upper limb
median
Lesion, nerve, median
ulnar
Lesion, nerve, ulnar
leg
Mononeuropathy, lower limb
median
Lesion, nerve, median
plantar
Lesion, nerve, plantar
ulnar
Lesion, nerve, ulnar
Angiospastic disease or edema
I73.9
Anisakiasis
(infection) (infestation)
B81.0
Anisakis larvae infestation
B81.0
Ankylosis
(fibrous) (osseous) (joint)
M24.60
cricoarytenoid
(cartilage) (joint) (larynx)
J38.7
incostapedial joint
(infectional)
Ankylosis, ear ossicles
jaw
(temporomandibular)
M26.61-
postoperative
(status)
Z98.1
produced by surgical fusion, status
Z98.1
spine
(joint)
Fusion, spine
spondylitic
Spondylitis, ankylosing
tooth, teeth
(hard tissues)
K03.5
Anodontia
(complete) (partial) (vera)
K00.0
Anomaly, anomalous
(congenital) (unspecified type)
Q89.9
Alder
(-Reilly) (leukocyte granulation)
D72.0
coarctation
(preductal) (postductal)
Q25.1
aortic cusp or valve
Q23.9
with spina bifida
Spina bifida, with hydrocephalus
aryteno-epiglottic folds
Q31.8
causing impairment of hearing
Q16.9
biliary duct or passage
Q44.5
supravesical fissure
Q64.11
encephalocele
Encephalocele
with spina bifida
Spina bifida, by site, with hydrocephalus
cardiovascular system
Q28.8
Chédiak-Higashi
(-Steinbrinck) (congenital gigantism of peroxidase granules)
E70.330
chromosomes, chromosomal
Q99.9
D
(1)
condition, chromosome 13
E
(3)
condition, chromosome 18
G
condition, chromosome 21
gonadal dysgenesis
(pure)
Q99.1
left ventricle with right atrium
Q21.0
renal artery with kidney
Q27.2
coronary artery or vein
Q24.5
alveolar
Anomaly, alveolar
alveolar
Anomaly, alveolar
dental arch relationship
M26.20
jaw-cranial base relationship
M26.10
dental arch relationship NEC
M26.29
jaw-cranial base relationship
Anomaly, dentofacial, jaw-cranial base relationship
jaw size
Anomaly, dentofacial, jaw size
temporomandibular joint
M26.60-
tooth position, fully erupted
M26.30
diaphragm NEC
(apertures)
Q79.1
digestive organ or tract
(s)
Q45.9
distance, interarch
(excessive) (inadequate)
M26.25
distribution, coronary artery
Q24.5
causing impairment of hearing
Q16.9
middle
(causing impairment of hearing)
Q16.4
Ebstein's
(heart) (tricuspid valve)
Q22.5
Eisenmenger's
(ventricular septal defect)
Q21.8
frontal bone
Anomaly, skull
gallbladder
(position) (shape) (size)
Q44.1
gastrointestinal tract
Q45.9
genitalia, genital organ or system
(s)
granulation or granulocyte, genetic
(constitutional) (leukocyte)
D72.0
hard tissue formation in pulp
K04.3
fibroelastosis cordis
I42.4
patent ductus arteriosus
(Botalli)
Q25.0
with pulmonary stenosis or atresia, dextraposition of aorta and hypertrophy of right ventricle
Q21.3
with pulmonary stenosis or atresia, dextraposition of aorta and hypertrophy of right ventricle
Q21.3
hypersegmentation of neutrophils, hereditary
D72.0
ileocecal
(coil) (valve)
Q43.9
interarch distance
(excessive) (inadequate)
M26.25
intervertebral cartilage or disc
Q76.49
intestine
(large) (small)
Q43.9
with anomalous adhesions, fixation or malrotation
Q43.3
alveolar
Anomaly, alveolar
jaw-cranial base relationship
Anomaly, dentofacial, jaw-cranial base relationship
kidney
(s) (calyx) (pelvis)
Q63.9
Klippel-Feil
(brevicollis)
Q76.1
labium
(majus) (minus)
Q52.70
labyrinth, membranous
Q16.5
lacrimal apparatus or duct
Q10.6
larynx, laryngeal
(muscle)
Q31.9
granulation
(constitutional)
D72.0
reduction deformity
Defect, reduction, lower limb
lumbosacral
(joint) (region)
Q76.49
kyphosis
Kyphosis, congenital
lordosis
Lordosis, congenital
lung
(fissure) (lobe)
Q33.9
mandible
Anomaly, dentofacial
maxilla
Anomaly, dentofacial
meatus urinarius NEC
Q64.79
meningeal bands or folds
Q07.9
mitral
(leaflets) (valve)
Q23.9
Müllerian
Anomaly, by site
musculoskeletal system, except limbs
Q79.9
nervous system
(central)
Q07.9
nose, nasal
(bones) (cartilage) (septum) (sinus)
Q30.9
omphalomesenteric duct
Q43.0
opening, pulmonary veins
Q26.4
opticociliary vessels
Q13.2
palate NEC
(hard) (soft)
Q38.5
pancreas or pancreatic duct
Q45.3
Pelger-Huët
(hereditary hyposegmentation)
D72.0
peripheral vascular system
Q27.9
position, tooth, teeth, fully erupted
M26.30
Argyll Robertson pupil
H57.01
reduction
(extremity) (limb)
femur
(longitudinal)
Defect, reduction, lower limb, longitudinal, femur
fibula
(longitudinal)
Defect, reduction, lower limb, longitudinal, fibula
lower limb
Defect, reduction, lower limb
radius
(longitudinal)
Defect, reduction, upper limb, longitudinal, radius
tibia
(longitudinal)
Defect, reduction, lower limb, longitudinal, tibia
ulna
(longitudinal)
Defect, reduction, upper limb, longitudinal, ulna
upper limb
Defect, reduction, upper limb
refraction
Disorder, refraction
sacroiliac NEC
(joint)
Q74.2
kyphosis
Kyphosis, congenital
lordosis
Lordosis, congenital
saddle nose, syphilitic
A50.57
salivary duct or gland
Q38.4
scrotum
Malformation, testis and scrotum
sex chromosomes NEC
Anomaly, chromosomes
shoulder
(girdle) (joint)
Q74.0
skeleton generalized
Q78.9
encephalocele
Encephalocele
with spina bifida
Spina bifida, by site, with hydrocephalus
specified organ or site NEC
Q89.8
kyphosis
Kyphosis, congenital
lordosis
Lordosis, congenital
testis
Malformation, testis and scrotum
position, fully erupted
M26.30
spacing, fully erupted
M26.30
tricuspid
(leaflet) (valve)
Q22.9
Uhl's
(hypoplasia of myocardium, right ventricle)
Q24.8
cricoid cartilage and thyroid cartilage
Q31.8
thyroid cartilage and hyoid bone
Q31.8
orthotopic ureterocele
Q62.31
with only one functioning horn
Q51.4
venae cavae inferioris
Q24.8
vein
(s) (peripheral)
Q27.9
vena cava
(inferior) (superior)
Q26.9
kyphosis
Kyphosis, congenital
lordosis
Lordosis, congenital
vesicourethral orifice
Q64.79
vitreous body or humor
Q14.0