ZFIN Human Disease: autosomal recessive intellectual developmental disorder 39

OBO ID: DOID:0081204

Term Name:	autosomal recessive intellectual developmental disorder 39		Search Ontology:
Synonyms:
Definition:	An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the TTI2 gene on chromosome 8p12. https://pubmed.ncbi.nlm.nih.gov/23956177/
References:	OMIM:615541
Ontology:	Human Disease ( DOID:0081204 )

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 39 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
TTI2	tti2	Intellectual developmental disorder, autosomal recessive 39	615541

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None