ORPHA:99941

Autosomal dominant Charcot-Marie-Tooth disease type 2G

Synonyms: CMT2G

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Charcot-Marie-Tooth disease type 2P

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Autosomal dominant Charcot-Marie-Tooth disease type 2G	CMT2G
fr	Maladie de Charcot-Marie-Tooth autosomique dominante type 2G	= en
de	Charcot-Marie-Tooth-Krankheit, autosomal-dominante, Typ 2G	= en
es	Enfermedad de Charcot-Marie-Tooth autosómica dominante tipo 2G
it	Malattia di Charcot-Marie-Tooth autosomica dominante, tipo 2G	= en
nl	Autosomaal dominante ziekte van Charcot-Marie-Tooth type 2G	= en
pt	Doença de Charcot-Marie-Tooth autossómica dominante tipo 2G
pl	Autosomalna dominująca choroba Charcota, Mariego i Tootha typu 2G	= en
cs	Autozomálně dominantní Charcotova-Marieova-Toothova nemoc, typ 2G	CMT2G · Autozomálně dominantní Charcot-Marie-Toothova nemoc, typ 2G
uk	Аутосомно-домінантна хвороба Шарко-Марі-Тута, тип 2G	= en
zh	常染色体显性遗传腓骨肌萎缩症2G型	= en
tr	Otozomal dominant Charcot-Marie-Tooth hastalığı tip 2G	= en

Definition in:

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
UMLS	C1837805	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Not placed in any Orphanet classification in this release.

No children.

0 direct

Orphanet records no gene directly on this code.

0 records

No prevalence record in this release.

Orphanet has no HPO annotation for this code in this release.