ZFIN Human Disease: autosomal recessive intellectual developmental disorder 2

OBO ID: DOID:0081178

Term Name:	autosomal recessive intellectual developmental disorder 2		Search Ontology:
Synonyms:
Definition:	An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the gene encoding cereblon (CRBN) on chromosome 3p26. https://pubmed.ncbi.nlm.nih.gov/28143899/
References:	OMIM:607417
Ontology:	Human Disease ( DOID:0081178 )

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 2 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CRBN	crbn	Intellectual developmental disorder, autosomal recessive 2	607417

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None