ZFIN Human Disease: split hand-foot malformation 6

OBO ID: DOID:0090026

Term Name:	split hand-foot malformation 6		Search Ontology:
Synonyms:	SHFM6
Definition:	A split-hand/foot malformation that has_material_basis_in homozygous mutation in the WNT10B gene on chromosome 12q13. https://www.ncbi.nlm.nih.gov/pubmed/18515319
References:	MESH:C574275 NCI:C75000 OMIM:225300 ORDO:2440 SNOMEDCT_US_2023_03_01:81208006 UMLS_CUI:C0265554
Ontology:	Human Disease ( DOID:0090026 )

Relationships

is a type of:	autosomal recessive disease split hand-foot malformation autosomal recessive disease split hand-foot malformation Show first 5 Terms

OTHER split hand-foot malformation 6 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
WNT10B	wnt10b	Split-hand/foot malformation 6	225300

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None