Term Name: cataract 9 multiple types
Synonyms: autosomal recessive congenital cataract 1, cataract 9 multiple types with or without microcornea, CATC1, CTRCT9
Definition: A cataract that has_material_basis_in autosomal recessive or autosomal dominant inheritance of heterozygous or homozygous mutation in the CRYAA gene, which encodes alpha-A-crystallin, on chromosome 21q22.
Ontology: Human Disease [DOID:0110266]   ( DOID:0110266 )

Relationships
is a type of: autosomal dominant disease autosomal recessive disease cataract