ZFIN Human Disease: autosomal recessive intellectual developmental disorder 3

OBO ID: DOID:0081179

Term Name:	autosomal recessive intellectual developmental disorder 3		Search Ontology:
Synonyms:
Definition:	An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the CC2D1A gene on chromosome 19p13. https://pubmed.ncbi.nlm.nih.gov/16033914/
References:	OMIM:608443
Ontology:	Human Disease ( DOID:0081179 )

Relationships

is a type of:	autosomal recessive intellectual developmental disorder autosomal recessive intellectual developmental disorder Show first 5 Terms

OTHER autosomal recessive intellectual developmental disorder 3 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CC2D1A	cc2d1a	Intellectual developmental disorder, autosomal recessive 3	608443

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None