ZFIN Human Disease: erythrokeratodermia variabilis et progressiva 1

OBO ID: DOID:0111195

Term Name:	erythrokeratodermia variabilis et progressiva 1		Search Ontology:
Synonyms:
Definition:	An erythrokeratodermia variabilis that has_material_basis_in heterozygous, homozygous, or compound heterozygous mutation in GJB3 on 1p34.3. (2)
References:	OMIM:133200
Ontology:	Human Disease ( DOID:0111195 )

Relationships

is a type of:	autosomal dominant disease autosomal recessive disease erythrokeratodermia variabilis autosomal dominant disease autosomal recessive disease erythrokeratodermia variabilis Show first 5 Terms

OTHER erythrokeratodermia variabilis et progressiva 1 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
GJB3	gjb3	Erythrokeratodermia variabilis et progressiva 1	133200

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None