DISEASES

Disease-gene associations mined from literature

Human genes for polyneuropathy

Polyneuropathy [DOID:1389]

A color blindness that is characterized by a congenital color vision disorder, the inability to perceive color and to achieve satisfactory visual acuity at high light levels has_material_basis_in autosomal recessive inheritance.

Synonyms:  polyneuropathy,  DOID:1389,  Polyneuropathy (disorder),  Polyneuropathy unspecified,  Polyneuropathy unspecified (disorder) ...

Linkouts:  OMIM #1 #2