ZFIN Human Disease: Charcot-Marie-Tooth disease axonal type 2P

OBO ID: DOID:0110169

Term Name:	Charcot-Marie-Tooth disease axonal type 2P		Search Ontology:
Synonyms:	Charcot-Marie-Tooth disease type 2P Charcot-Marie-Tooth neuropathy type 2P CMT2P
Definition:	A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or heterozygous mutation in the LRSAM1 gene on chromosome 9q33. https://www.ncbi.nlm.nih.gov/pubmed/20865121
References:	GARD:12435 ICD10CM:G60.0 OMIM:614436 ORDO:300319
Ontology:	Human Disease ( DOID:0110169 )

Relationships

is a type of:	autosomal dominant disease autosomal recessive disease Charcot-Marie-Tooth disease type 2 autosomal dominant disease autosomal recessive disease Charcot-Marie-Tooth disease type 2 Show first 5 Terms

OTHER Charcot-Marie-Tooth disease axonal type 2P PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
LRSAM1	lrsam1	Charcot-Marie-Tooth disease, axonal, type 2P	614436

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None