ZFIN Human Disease: cataract 9 multiple types

OBO ID: DOID:0110266

Term Name:	cataract 9 multiple types		Search Ontology:
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. (2)
References:	ICD10CM:Q12.0 OMIM:604219
Ontology:	Human Disease ( DOID:0110266 )

Relationships

is a type of:	autosomal dominant disease autosomal recessive disease cataract autosomal dominant disease autosomal recessive disease cataract Show first 5 Terms

OTHER cataract 9 multiple types PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CRYAA	cryaa	Cataract 9, multiple types	604219

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None