ZFIN Human Disease: autosomal recessive intellectual developmental disorder 12

OBO ID: DOID:0081180

Term Name:	autosomal recessive intellectual developmental disorder 12		Search Ontology:
Synonyms:
Definition:	An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the ST3GAL3 gene on chromosome 1p34. https://pubmed.ncbi.nlm.nih.gov/32666583/
References:	OMIM:611090
Ontology:	Human Disease ( DOID:0081180 )

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 12 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ST3GAL3	st3gal3a st3gal3b	Intellectual developmental disorder, autosomal recessive 12	611090

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None