ZFIN Human Disease: autosomal recessive intellectual developmental disorder 46

OBO ID: DOID:0081210

Term Name:	autosomal recessive intellectual developmental disorder 46		Search Ontology:
Synonyms:
Definition:	An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the NDST1 gene on chromosome 5q33. https://pubmed.ncbi.nlm.nih.gov/25125150/
References:	OMIM:616116
Ontology:	Human Disease ( DOID:0081210 )

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 46 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
NDST1	ndst1b ndst1a	Intellectual developmental disorder, autosomal recessive 46	616116

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None