ZFIN Human Disease: autosomal recessive intellectual developmental disorder 47

OBO ID: DOID:0081211

Term Name:	autosomal recessive intellectual developmental disorder 47		Search Ontology:
Synonyms:
Definition:	An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the FMN2 gene on chromosome 1q43. https://pubmed.ncbi.nlm.nih.gov/25480035/
References:	OMIM:616193
Ontology:	Human Disease ( DOID:0081211 )

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 47 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
FMN2	fmn2a fmn2b	Intellectual developmental disorder, autosomal recessive 47	616193

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None