ZFIN Human Disease: autosomal recessive intellectual developmental disorder 1

OBO ID: DOID:0081177

Term Name:	autosomal recessive intellectual developmental disorder 1		Search Ontology:
Synonyms:
Definition:	An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the gene encoding neurotrypsin (PRSS12) on chromosome 4q25. https://pubmed.ncbi.nlm.nih.gov/12459588/
References:	OMIM:249500
Ontology:	Human Disease ( DOID:0081177 )

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 1 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
PRSS12	prss12	Intellectual developmental disorder, autosomal recessive 1	249500

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None