Hereditary Coproporphyria

An autosomal dominant inherited disorder of porphyrin metabolism caused by deficiency of the enzyme coproporphyrinogen oxidase. It results in neurologic damage and can include abdominal pain, constipation and psychiatric manifestations. (NCI Thesaurus)

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Hereditary Connective Tissue Disorder

An inherited genetic disorder that affects the connective tissues. Representative examples include Ehlers-Danlos syndrome and Marfan syndrome.

Hereditary Coagulation Factor Deficiency

An inherited blood coagulation disorder characterized by deficiency of one of the coagulation factors, resulting in bleeding.

Hereditary Clear Cell Renal Cell Carcinoma

A manifestation of von Hippel-Lindau disease or other familial renal cell cancer syndromes that present as a malignant epithelial neoplasm of the…

Hereditary cancer syndrome

A type of inherited disorder in which there is a higher-than-normal risk of certain types of cancer. Hereditary cancer syndromes are caused…

Hereditary Breast Carcinoma

Breast carcinoma that has developed in relatives of patients with history of breast carcinoma.

Hereditary breast and ovarian cancer syndrome

An inherited disorder in which the risk of breast cancer (especially before the age of 50) and ovarian cancer is higher than…