ZFIN Human Disease: autosomal recessive intellectual developmental disorder 38

OBO ID: DOID:0081203

Term Name:	autosomal recessive intellectual developmental disorder 38		Search Ontology:
Synonyms:
Definition:	An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the HERC2 gene on chromosome 15q13. https://pubmed.ncbi.nlm.nih.gov/23243086/
References:	OMIM:615516
Ontology:	Human Disease ( DOID:0081203 )

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 38 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
HERC2	herc2	Intellectual developmental disorder, autosomal recessive 38	615516

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None