ZFIN Human Disease: Sotos syndrome 3

OBO ID: DOID:0112104

Term Name:	Sotos syndrome 3		Search Ontology:
Synonyms:	SOTOS3
Definition:	A Sotos syndrome that has_material_basis_in homozygous mutation in the APC2 gene on chromosome 19p13.3. https://pubmed.ncbi.nlm.nih.gov/25753423/
References:	OMIM:617169
Ontology:	Human Disease ( DOID:0112104 )

Relationships

is a type of:	autosomal recessive disease Sotos syndrome autosomal recessive disease Sotos syndrome Show first 5 Terms

OTHER Sotos syndrome 3 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
APC2	apc2	Intellectual developmental disorder, autosomal recessive 74	617169

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None