Diseases

T85830D

Hemorrhage due to nervous system prosthetic devices, implants and grafts, subsequent encounter

T85838A

Hemorrhage due to other internal prosthetic devices, implants and grafts, initial encounter

T85838S

Hemorrhage due to other internal prosthetic devices, implants and grafts, sequela

T85838D

Hemorrhage due to other internal prosthetic devices, implants and grafts, subsequent encounter

T82838A

Hemorrhage due to vascular prosthetic devices, implants and grafts, initial encounter

T82838S

Hemorrhage due to vascular prosthetic devices, implants and grafts, sequela

T82838D

Hemorrhage due to vascular prosthetic devices, implants and grafts, subsequent encounter

R0489

Hemorrhage from other sites in respiratory passages

R049

Hemorrhage from respiratory passages, unspecified

R041

Hemorrhage from throat

J9501

Hemorrhage from tracheostomy stoma

O209

Hemorrhage in early pregnancy, unspecified

H47023

Hemorrhage in optic nerve sheath, bilateral

H47022

Hemorrhage in optic nerve sheath, left eye

H47021

Hemorrhage in optic nerve sheath, right eye

H47029

Hemorrhage in optic nerve sheath, unspecified eye

K625

Hemorrhage of anus and rectum

H05233

Hemorrhage of bilateral orbit

N99530

Hemorrhage of continent stoma of urinary tract

N99520

Hemorrhage of incontinent external stoma of urinary tract

H05232

Hemorrhage of left orbit

H05231

Hemorrhage of right orbit

H05239

Hemorrhage of unspecified orbit

R58

Hemorrhage, not elsewhere classified

H31413

Hemorrhagic choroidal detachment, bilateral

H31412

Hemorrhagic choroidal detachment, left eye

H31411

Hemorrhagic choroidal detachment, right eye

H31419

Hemorrhagic choroidal detachment, unspecified eye

D699

Hemorrhagic condition, unspecified

H35733

Hemorrhagic detachment of retinal pigment epithelium, bilateral

H35732

Hemorrhagic detachment of retinal pigment epithelium, left eye

H35731

Hemorrhagic detachment of retinal pigment epithelium, right eye

H35739

Hemorrhagic detachment of retinal pigment epithelium, unspecified eye

P53

Hemorrhagic disease of newborn

D6832

Hemorrhagic disorder due to extrinsic circulating anticoagulants

A985

Hemorrhagic fever with renal syndrome

H60323

Hemorrhagic otitis externa, bilateral

H60322

Hemorrhagic otitis externa, left ear

H60321

Hemorrhagic otitis externa, right ear

H60329

Hemorrhagic otitis externa, unspecified ear

O2241

Hemorrhoids in pregnancy, first trimester

O2242

Hemorrhoids in pregnancy, second trimester

O2243

Hemorrhoids in pregnancy, third trimester

O2240

Hemorrhoids in pregnancy, unspecified trimester

O872

Hemorrhoids in the puerperium

J942

Hemothorax

D75829

Heparin-induced thrombocytopenia, unspecified

K7682

Hepatic encephalopathy

K7291

Hepatic failure, unspecified with coma

K7290

Hepatic failure, unspecified without coma

K742

Hepatic fibrosis with hepatic sclerosis

K7402

Hepatic fibrosis, advanced fibrosis

K7401

Hepatic fibrosis, early fibrosis

K7400

Hepatic fibrosis, unspecified

K741

Hepatic sclerosis

K765

Hepatic veno-occlusive disease

B150

Hepatitis A with hepatic coma

B159

Hepatitis A without hepatic coma

C222

Hepatoblastoma

R162

Hepatomegaly with splenomegaly, not elsewhere classified

R160

Hepatomegaly, not elsewhere classified

K7681

Hepatopulmonary syndrome

K767

Hepatorenal syndrome

O9041

Hepatorenal syndrome following labor and delivery

C8610

Hepatosplenic T-cell lymphoma not having achieved remission

C8611

Hepatosplenic T-cell lymphoma, in remission

D8944

Hereditary alpha tryptasemia

G609

Hereditary and idiopathic neuropathy, unspecified

G119

Hereditary ataxia, unspecified

H3120

Hereditary choroidal dystrophy, unspecified

D682

Hereditary deficiency of other clotting factors

K005

Hereditary disturbances in tooth structure, not elsewhere classified

D581

Hereditary elliptocytosis

E800

Hereditary erythropoietic porphyria

D67

Hereditary factor IX deficiency

D66

Hereditary factor VIII deficiency

D681

Hereditary factor XI deficiency

E7412

Hereditary fructose intolerance

E83110

Hereditary hemochromatosis

D589

Hereditary hemolytic anemia, unspecified

D5932

Hereditary hemolytic-uremic syndrome

I780

Hereditary hemorrhagic telangiectasia

D800

Hereditary hypogammaglobulinemia

Q820

Hereditary lymphedema

G600

Hereditary motor and sensory neuropathy

N07B

Hereditary nephropathy, not elsewhere classified with APOL1-mediated kidney disease [AMKD]

N07A

Hereditary nephropathy, not elsewhere classified with C3 glomerulonephritis

N076

Hereditary nephropathy, not elsewhere classified with dense deposit disease

N077

Hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritis

N074

Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritis

N072

Hereditary nephropathy, not elsewhere classified with diffuse membranous glomerulonephritis

N073

Hereditary nephropathy, not elsewhere classified with diffuse mesangial proliferative glomerulonephritis

N075

Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis

N071

Hereditary nephropathy, not elsewhere classified with focal and segmental glomerular lesions

N070

Hereditary nephropathy, not elsewhere classified with minor glomerular abnormality

N078

Hereditary nephropathy, not elsewhere classified with other morphologic lesions

N079

Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesions

H4722

Hereditary optic atrophy

D564

Hereditary persistence of fetal hemoglobin [HPFH]

D640

Hereditary sideroblastic anemia