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Rare Disease Database

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Hailey-Hailey Disease

Haim-Munk Syndrome

Hajdu Cheney Syndrome

Hallermann Streiff Syndrome

Hand-Foot-Mouth Syndrome

Hanhart Syndrome

Hantavirus Pulmonary Syndrome

Hartnup Disease

Hay-Wells Syndrome

Heart Block, Congenital

Heavy Metal Poisoning

Hematuria, Benign, Familial

Hemimegalencephaly

Hemophilia A

Hemophilia B

Hemorrhagic Telangiectasia, Hereditary

Henoch-Schönlein Purpura

Hepatic Encephalopathy

Hepatic Fibrosis, Congenital

Hepatitis B

Hepatorenal Syndrome

Hereditary Hyperphosphatasia

Hereditary Lymphedema

Hereditary Multiple Osteochondromas

Hereditary Spastic Paraplegia

Hermansky Pudlak syndrome

Herpes, Neonatal

Hers Disease

Hiccups, Chronic

Hidradenitis Suppurativa

Hirschsprung's Disease

Histidinemia

Hodgkin's Disease

Holoprosencephaly

Holt Oram Syndrome

Homocystinuria due to Cystathionine Beta-Synthase Deficiency

Horner's Syndrome

HTLV Type I and Type II

Human Granulocytic Ehrlichiosis (HGE)

Human HOXA1 Syndromes

Human Monocytic Ehrlichiosis (HME)

Hunter Syndrome

Huntington's Disease

Hydranencephaly

Hydrocephalus

Hyperekplexia

Hyperemesis Gravidarum

Hyperferritinemia Cataract Syndrome

Hyperhidrosis, Primary

Hyper IgD syndrome

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