Results 1 -
10
of
113
for
Hereditary disease
- ... In these cases, the condition is sometimes called hereditary desmoid disease. Aggressive fibromatosis Deep fibromatosis Desmoid fibromatosis Familial infiltrative ...
- ... C3 inactivator deficiency Complement component 3 inactivator deficiency Hereditary factor I deficiency disease Genetic Testing Registry: Hereditary factor I deficiency disease ...
- ... activation of phospholipase C-gamma2 in the human hereditary disease PLAID. Cell Signal. 2016 Sep;28(9):1237- ...
- ... FAP MYH-associated polyposis Genetic Testing Registry: Desmoid disease, hereditary Genetic Testing Registry: Familial adenomatous polyposis 1 Genetic ...
- ... Registry: Charcot-Marie-Tooth disease Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy National Organization for Rare ... DISEASE, X-LINKED RECESSIVE, 5; CMTX5 ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D; CMT2D CHARCOT-MARIE-TOOTH DISEASE, ...
- ... repeats or more). Huntington chorea Huntington chronic progressive hereditary chorea Huntington disease Huntington's chorea Genetic Testing Registry: Juvenile Huntington ...
- ... family, the condition is described as Meige-like disease. Hereditary lymphedema II Late-onset lymphedema LMPH2 Lymphedema praecox Meige lymphedema Genetic Testing Registry: Lymphedema praecox Meige disease National Organization for Rare Disorders (NORD) ClinicalTrials.gov ...
- ... Testing Registry: Hemophilia b(m) Genetic Testing Registry: Hereditary factor IX deficiency disease Genetic Testing Registry: Hereditary factor VIII deficiency disease ...
- ... deficiency disease, HDL, familial Tangier disease neuropathy Tangier hereditary neuropathy Genetic Testing Registry: Tangier disease Tangier disease National Organization for Rare Disorders (NORD) ...
- ... one eye has the hereditary or the non-hereditary form of the disease. Glioma, retinal RB Genetic Testing Registry: Retinoblastoma Retinoblastoma ...
