ZFIN Human Disease: autosomal recessive intellectual developmental disorder 51

OBO ID: DOID:0081214

Term Name:	autosomal recessive intellectual developmental disorder 51		Search Ontology:
Synonyms:
Definition:	An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the HNMT gene on chromosome 2q22. https://pubmed.ncbi.nlm.nih.gov/26206890/
References:	OMIM:616739
Ontology:	Human Disease ( DOID:0081214 )

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 51 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
HNMT	hnmt	Intellectual developmental disorder, autosomal recessive 51	616739

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None