ZFIN Human Disease: Klippel-Feil syndrome 2

OBO ID: DOID:0080590

Term Name:	Klippel-Feil syndrome 2		Search Ontology:
Synonyms:
Definition:	A Klippel-Feil syndrome that has_material_basis_in homozygous mutation in the MEOX1 gene on chromosome 17q21. https://www.ncbi.nlm.nih.gov/pubmed/23290072
References:	OMIM:214300
Ontology:	Human Disease ( DOID:0080590 )

Relationships

is a type of:	autosomal recessive disease Klippel-Feil syndrome autosomal recessive disease Klippel-Feil syndrome Show first 5 Terms

OTHER Klippel-Feil syndrome 2 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
MEOX1	meox1	Klippel-Feil syndrome 2	214300

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None