Congenital afibrinogenemia or familial afibrinogenemia is a rare, genetically inherited blood fibrinogen disorder in which the blood does not clot normally due...
Rare
Adenosine deaminase deficiency (ADA deficiency) is a rare disease with an incidence of <1 case per 100,000 live births worldwide,...
Acrospiroma (Know as Hidradenoma or Eccrine Acrospiroma) too, is a rare cutaneous tumor of the eccrine sweat gland which occurs primarily in adult...
Acute lymphoblastic leukemia (ALL) is a rare type of cancer that affects the lymphoid line of blood cells and characterized...
Acute intermittent porphyria (AIP) is a rare metabolic disorder that affects heme production as a result of porphobilinogen deaminase deficiency....
Acromegaly is a rare non-cancerous tumor (Adenoma) disorder where the pituitary gland produces too much growth hormone, causing body tissues and bones to...
Acral lentiginous melanoma is a kind of lentiginous skin melanoma. “lentiginous” means that the spot of melanoma is much darker...
