ZFIN Human Disease: autosomal recessive intellectual developmental disorder 76

OBO ID: DOID:0081235

Term Name:	autosomal recessive intellectual developmental disorder 76		Search Ontology:
Synonyms:
Definition:	An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the GRIA1 gene on chromosome 5q33. https://pubmed.ncbi.nlm.nih.gov/35675825/
References:	OMIM:619931
Ontology:	Human Disease ( DOID:0081235 )

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 76 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
GRIA1	gria1a gria1b	?Intellectual developmental disorder, autosomal recessive 76	619931

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None