GARD Rare Disease Listings

Heart defect-tongue hamartoma-polysyndactyly syndrome

Also known as: Ostravik-Lindemann-Solberg syndrome Congenital heart defects, hamartomas of tongue, and polysyndactyly Orstavik Lindemann Solberg syndrome

Heart tumor

Also known as: Myocardial tumors (rhabdomyomas and fibromas) Intracavitary tumors Primary cardiac tumors, childhood

Heart-hand syndrome, Slovenian type

Heart-hand syndrome, Spanish type

Also known as: Brachydactyly and intraventricular conduction defect Upper limb malformations and congenital cardiac anomalies

Heavy metal poisoning

Also known as: Chronic heavy metal poisoning Heavy Metal Toxicity

HEC syndrome

Also known as: Hydrocephalus, endocardial fibroelastosis, and cataracts Communicating hydrocephalus, endocardial fibroelastosis (EFE) and congenital cataracts

Heinz body anemias

HELLP syndrome

Also known as: Hemolysis, Elevated Liver Enzymes, Lowered Platelets

Helminthiasis

Also known as: Intestinal helminthiasis

Hemangioblastoma

Hemangioendothelioma

Hemangioma thrombocytopenia syndrome

Also known as: Kasabach Merritt syndrome Thrombocytopenia-hemangioma syndrome Kasabach Merritt phenomenon KMP

Hemangiomatosis, familial pulmonary capillary

Also known as: Familial pulmonary capillary hemangiomatosis

Hemangiopericytoma

Hematohidrosis

Also known as: Hematidrosis