ZFIN Human Disease: Charcot-Marie-Tooth disease type 3

OBO ID: DOID:0050540

Term Name:	Charcot-Marie-Tooth disease type 3		Search Ontology:
Synonyms:	DEJERINE-SOTTAS NEUROPATHY DEJERINE-SOTTAS SYNDROME
Definition:	A Charcot-Marie-Tooth disease that is characterized by motor and sensory peripheral neuropathies caused by demyelination. https://en.wikipedia.org/wiki/Charcot%E2%80%93Marie%E2%80%93Tooth_disease
References:	OMIM:145900
Ontology:	Human Disease ( DOID:0050540 )

Relationships

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

OTHER Charcot-Marie-Tooth disease type 3 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
EGR2	egr2b egr2a	Dejerine-Sottas disease	145900
MPZ	mpz	Dejerine-Sottas disease	145900
PMP22	pmp22a pmp22b	Dejerine-Sottas disease	145900
PRX	prx	Dejerine-Sottas disease	145900

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None