ZFIN Human Disease: autosomal recessive intellectual developmental disorder 59

OBO ID: DOID:0081221

Term Name:	autosomal recessive intellectual developmental disorder 59		Search Ontology:
Synonyms:
Definition:	An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the IMPA1 gene on chromosome 8q21. https://pubmed.ncbi.nlm.nih.gov/26416544/
References:	OMIM:617323
Ontology:	Human Disease ( DOID:0081221 )

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 59 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
IMPA1	impa1	Intellectual developmental disorder, autosomal recessive 59	617323

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None