Terms Related to Yellow Mutant Albinism

• Ocular Albinism

  Albinism affecting the eye in which pigment of the hair and skin is normal or only slightly diluted. The classic type is X-linked (Nettleship-Falls), but ...

• Albinism

  General term for a number of inherited defects of amino acid metabolism in which there is a deficiency or absence of pigment in the eyes, ...

• Cystadenocarcinoma

  A malignant neoplasm derived from glandular epithelium, in which cystic accumulations of retained secretions are formed. The neoplastic cells manifest varying degrees of anaplasia and ...

• Hyperphenylalaninaemia

  A group of autosomal recessive disorders marked by a deficiency of the hepatic enzyme PHENYLALANINE HYDROXYLASE or less frequently by reduced activity of DIHYDROPTERIDINE REDUCTASE ...

• Chediak Higashi Syndrome

  A form of phagocyte bactericidal dysfunction characterized by unusual oculocutaneous albinism, high incidence of lymphoreticular neoplasms, and recurrent pyogenic infections. In many cell types, abnormal ...

• Dihydropteridine Reductase Deficiency Disease

  A group of autosomal recessive disorders marked by a deficiency of the hepatic enzyme PHENYLALANINE HYDROXYLASE or less frequently by reduced activity of DIHYDROPTERIDINE REDUCTASE ...

• Chondrodystrophia Calcificans Congenita

  A heterogeneous group of bone dysplasias, the common character of which is stippling of the epiphyses in infancy. The group includes a severe autosomal recessive ...