Hoffmann-Bouveret syndrome
I47.9
Hollenhorst's plaque
Occlusion, artery, retina
Homocystinemia, homocystinuria
E72.11
Homogentisate 1,2-dioxygenase deficiency
E70.29
Homologous serum hepatitis
(prophylactic) (therapeutic)
Hepatitis, viral, type B
Hookworm
(anemia) (disease) (infection) (infestation)
B76.9
Hordeolum
(eyelid) (externum) (recurrent)
H00.019
Horton's headache or neuralgia
G44.099
Household, housing circumstance affecting care
Z59.9
Hudson
(-Stähli) line (cornea)
Pigmentation, cornea, anterior
Humidifier lung or pneumonitis
J67.7
Hunner's ulcer
Cystitis, chronic, interstitial
Huntington's disease or chorea
G10
with behavioral disturbance
G10
F02.81
Hurler disease or syndrome
(-Scheie)
E76.02
Hutchinson-Boeck disease or syndrome
Sarcoidosis
Hutchinson-Gilford disease or syndrome
E34.8
Hyalin plaque, sclera, senile
H15.89
Hyaline membrane
(disease) (lung) (pulmonary) (newborn)
P22.0
Hyalitis, hyalosis, asteroid
Deposit, crystalline
Hydatidiform mole
(benign) (complicating pregnancy) (delivered) (undelivered)
O01.9
Hydradenitis
(axillaris) (suppurative)
L73.2
Hydrancephaly, hydranencephaly
Q04.3
with spina bifida
Spina bifida, with hydrocephalus
Hydroadenitis
(axillaris) (suppurative)
L73.2
Hydrocele
(spermatic cord) (testis) (tunica vaginalis)
N43.3
Hydrocephalus
(acquired) (external) (internal) (malignant) (recurrent)
G91.9
aqueduct Sylvius stricture
Q03.0
causing disproportion
O33.6
with obstructed labor
O66.3
congenital
(external) (internal)
Q03.9
due to toxoplasmosis
(congenital)
P37.1
foramen Magendie block
(acquired)
G91.1
congenital
Q03.1
Hydrocephalus, congenital
infectious disease NEC
B89
G91.4
neoplastic disease NEC
(see also Neoplasm)
G91.4
parasitic disease
B89
G91.4
with spina bifida
Spina bifida, with hydrocephalus
syphilitic, congenital
A50.49
Hydroencephalomeningocele
(congenital)
Encephalocele
Hydronephrosis NEC
(atrophic) (early) (functionless) (intermittent) (primary) (secondary)
N13.30
ureteropelvic junction
(congenital)
Q62.11
ureteral stricture NEC
N13.1
due to acquired occlusion of ureteropelvic junction
N13.0
Hydrosadenitis
(axillaris) (suppurative)
L73.2
Hydrosalpinx
(fallopian tube) (follicularis)
N70.11
Hymenolepis, hymenolepiasis
(diminuta) (infection) (infestation) (nana)
B71.0
Hyperactive, hyperactivity
F90.9
basal cell, uterine cervix
Dysplasia, cervix
cervix epithelial
(basal)
Dysplasia, cervix
attention deficit
Disorder, attention-deficit hyperactivity
nasal mucous membrane
J34.3
thyroid
(gland)
Hyperthyroidism
Hypercalcemia, hypocalciuric, familial
E83.52
Hypercalciuria, idiopathic
R82.994
Hypercholesterolemia
(essential) (primary) (pure)
E78.00
with hyperglyceridemia, endogenous
E78.2
dietary counseling and surveillance
Z71.3
Hyperchylia gastrica, psychogenic
F45.8
Hypercorticalism, pituitary-dependent
E24.0
Hyperestrogenism
(drug-induced) (iatrogenic)
E28.0
Hyperglycemia, hyperglycemic
(transient)
R73.9
coma
Diabetes, by type, with coma
Hyperglyceridemia
(endogenous) (essential) (familial) (hereditary) (pure)
E78.1
Hyperhidrosis, hyperidrosis
R61
Hyperkinesia, hyperkinetic
(disease) (reaction) (syndrome) (childhood) (adolescence)
Disorder, attention-deficit hyperactivity
Hyperleucine-isoleucinemia
E71.19
Hyperlipemia, hyperlipidemia
E78.5
Hyperlucent lung, unilateral
J43.0
Hypermobility, hypermotility
cecum
Syndrome, irritable bowel
colon
Syndrome, irritable bowel
intestine
K58.9
Syndrome, irritable bowel
meniscus
(knee)
Derangement, knee, meniscus
scapula
Instability, joint, shoulder
with intrinsic sphincter deficiency
N36.43
Hyperostosis
(monomelic)
Disorder, bone, density and structure, specified NEC
cervicothoracic region
M48.13
occipito-atlanto-axial region
M48.11
sacrococcygeal region
M48.18
thoracolumbar region
M48.15
frontal, internal of skull
M85.2
skeletal, diffuse idiopathic
Hyperostosis, ankylosing
vertebral, ankylosing
Hyperostosis, ankylosing
Hyperpermeability, capillary
I78.8
Hyperphenylalaninemia NEC
E70.1
Hyperplasia, hyperplastic
adrenal
(capsule) (cortex) (gland)
E27.8
sexual precocity
(male)
E25.9
virilization
(female)
E25.9
angiolymphoid, eosinophilia
(ALHE)
D18.01
artery, fibromuscular
I77.3
breast
Hypertrophy, breast
cementation
(tooth) (teeth)
K03.4
cervix
(uteri) (basal cell) (endometrium) (polypoid)
Dysplasia, cervix
clitoris, congenital
Q52.6
endometrium, endometrial
(adenomatous) (benign) (cystic) (glandular) (glandular-cystic) (polypoid)
N85.00
complex
(without atypia)
N85.01
simple
(without atypia)
N85.01
focal, oral, including tongue
K13.29
fibromuscular of artery
(carotid) (renal)
I77.3
glandularis cystica uteri
(interstitialis)
N85.00-
Hyperplasia, endometrial
irritative, edentulous
(alveolar)
K06.2
mandible, mandibular
M26.03
myometrium, myometrial
N85.2
neuroendocrine cell, of infancy
J84.841
oral mucosa
(irritative)
K13.6
organ or site, congenital NEC
Anomaly, by site
palate, papillary
(irritative)
K13.6
pancreatic islet cells
E16.9
prostate
(adenofibromatous) (nodular)
N40.0
with lower urinary tract symptoms
(LUTS)
N40.1
without lower urinary tract symtpoms
(LUTS)
N40.0
reticulo-endothelial
(cell)
D75.89
Schimmelbusch's
Mastopathy, cystic
suprarenal capsule
(gland)
E27.8
thymus
(gland) (persistent)
E32.0
tonsils
(faucial) (infective) (lingual) (lymphoid)
J35.1
endometrium
(glandular)
N85.00-
Hyperplasia, endometrial
Hyperprebetalipoproteinemia
(familial)
E78.1
Hyperprothrombinemia, causing coagulation factor deficiency
D68.4
Hypersegmentation, leukocytic, hereditary
D72.0
Hypersensitive, hypersensitiveness, hypersensitivity
Allergy
pneumonitis
Pneumonitis, allergic
upper respiratory tract NEC
J39.3
Hypersplenia, hypersplenism
D73.1
Hyperstimulation, ovaries
(associated with induced ovulation)
N98.1
Hypertension, hypertensive
(accelerated) (benign) (essential) (idiopathic) (malignant) (systemic)
I10
heart failure
(congestive)
I11.0
heart involvement
(conditions in I50.-, I51.4- I51.9 due to hypertension)
Hypertension, heart
kidney involvement
Hypertension, kidney
benign, intracranial
G93.2
cardiorenal
(disease)
I13.10
with stage 1 through stage 4 chronic kidney disease
I13.0
with stage 5 or end stage renal disease
I13.2
without heart failure
I13.10
with stage 1 through stage 4 chronic kidney disease
I13.10
with stage 5 or end stage renal disease
I13.11
disease
(arteriosclerotic) (sclerotic)
Hypertension, heart
renal
(disease)
Hypertension, cardiorenal
chronic venous
Hypertension, venous (chronic)
with edema
O14.9-
Pre-eclampsia
gestational
(pregnancy induced) (without proteinuria)
O13.-
moderate pre-eclampsia
O14.0-
severe pre-eclampsia
O14.1-
with hemolysis, elevated liver enzymes and low platelet count
(HELLP)
O14.2-
with renal disease
O10.31-
with heart disease
O10.31-
puerperium, pre-existing
O16.5
renovascular disorders
I15.0
specified disease NEC
I15.8
gestational
(without significant proteinuria) (pregnancy-induced) (transient)
O13.-
with significant proteinuria
Pre-eclampsia
heart
(disease) (conditions in I51.4-I51.9 due to hypertension)
I11.9
heart failure
(congestive)
I11.0
kidney disease
(chronic)
Hypertension, cardiorenal
intracranial
(benign)
G93.2
heart disease
Hypertension, cardiorenal
stage 5 chronic kidney disease
(CKD) or end stage renal disease (ESRD)
I12.0
stage 1 through stage 4 chronic kidney disease
I12.9
pulmonary
(persistent)
P29.30
pancreatic duct - code to underlying condition
with chronic pancreatitis
K86.1
portal
(due to chronic liver disease) (idiopathic)
K76.6
in
(due to) schistosomiasis (bilharziasis)
B65.9
K77
cor pulmonale
(chronic)
I27.29
right heart ventricular strain/failure
I27.29
right to left shunt related to congenital heart disease
I27.83
unclear multifactorial mechanisms
I27.29
arterial
(associated) (drug-induced) (toxin-induced)
I27.21
chronic thromboembolic
I27.24
hematologic disorders
I27.29
lung diseases and hypoxia
I27.23
metabolic disorders
I27.29
specified systemic disorders NEC
I27.29
group 1
(associated) (drug-induced) (toxin-induced)
I27.21
of newborn
(persistent)
P29.30
renal
Hypertension, kidney
renovascular disorders
I15.0
deep vein thrombosis
Syndrome, postthrombotic
specified complication NEC
I87.39-
Hyperthyroidism
(latent) (pre-adult) (recurrent)
E05.90
nodular
(multinodular)
E05.20
due to ectopic thyroid tissue
E05.30
neonatal, transitory
P72.1
Hypertony, hypertonia, hypertonicity
uterus, uterine
(contractions) (complicating delivery)
O62.4
Hypertriglyceridemia, essential
E78.1
Hypertrophy, hypertrophic
adenofibromatous, prostate
Enlargement, enlarged, prostate
alveolar process or ridge
Anomaly, alveolar
auricular
Hypertrophy, cardiac
bile duct
(common) (hepatic)
K83.8
bladder
(sphincter) (trigone)
N32.89
puerperal, postpartum
Disorder, breast, specified type NEC
senile
(parenchymatous)
N62
cardiac
(chronic) (idiopathic)
I51.7
with rheumatic fever
(conditions in I00)
inactive or quiescent
(with chorea)
I09.89
fatty
Degeneration, myocardial
hypertensive
Hypertension, heart
rheumatic
(with chorea)
I09.89
cartilage
Disorder, cartilage, specified type NEC
clitoris
(cirrhotic)
N90.89
conjunctiva, lymphoid
H11.89
endometrium
(glandular)
N85.00-
Hyperplasia, endometrial
esophageal hiatus
(congenital)
Q79.1
with hernia
Hernia, hiatal
eyelid
Disorder, eyelid, specified type NEC
knee
(infrapatellar) (popliteal) (prepatellar) (retropatellar)
M79.4
frenulum, frenum
(tongue)
K14.8
gum
(mucous membrane)
K06.1
heart
(idiopathic)
Hypertrophy, cardiac
hepatic
Hypertrophy, liver
kidney
(compensatory)
N28.81
labium
(majus) (minus)
N90.60
ligament
Disorder, ligament
lingual tonsil
(infective)
J35.1
cirrhotic
Cirrhosis, liver
lymph, lymphatic gland
R59.9
tuberculous
Tuberculosis, lymph gland
mammary gland
Hypertrophy, breast
Meckel's diverticulum
(congenital)
Q43.0
malignant
Table of Neoplasms, small intestine, malignant
median bar
Hyperplasia, prostate
meniscus, knee, congenital
Q74.1
metatarsal head
Hypertrophy, bone, metatarsus
metatarsus
Hypertrophy, bone, metatarsus
muscular coat, artery
I77.89
myocardium
Hypertrophy, cardiac
mucous membrane
(septum)
J34.3
nasopharynx, lymphoid
(infectional) (tissue) (wall)
J35.2
organ or site, congenital NEC
Anomaly, by site
pancreas, congenital
Q45.3
lymphoid
(infectional) (tissue) (wall)
J35.2
pituitary
(anterior) (fossa) (gland)
E23.6
prostate
Enlargement, enlarged, prostate
pylorus
(adult) (muscle) (sphincter)
K31.1
congenital or infantile
Q40.0
rectal, rectum
(sphincter)
K62.89
scaphoid
(tarsal)
Hypertrophy, bone, tarsus
suprarenal cortex
(gland)
E27.8
tendon
Disorder, tendon, specified type NEC
thymic, thymus
(gland) (congenital)
E32.0
acquired
Deformity, toe, specified NEC
tonsils
(faucial) (infective) (lingual) (lymphoid)
J35.1
neck
(with elongation)
N88.4
ventricle, ventricular
(heart)
Hypertrophy, cardiac
in tetralogy of Fallot
Q21.3
stasis
(nonfilarial)
N90.69
Hypoadrenalism, hypoadrenia
E27.40
Hypochondria, hypochondriac, hypochondriasis
(reaction)
F45.21
Hypochromasia, blood cells
D50.8