Skip to
  1. Homepage
  2. Rare diseases
  3. Search
Simple search

Simple search

(*) mandatory field


Other search option(s)

Congenital muscular dystrophy type 1D

Synonym(s) MDC1D
Prevalence -
Inheritance -
Age of onset -
  • G71.2
MeSH -
MedDRA -


This disease has been moved to Congenital muscular dystrophy due to dystroglycanopathy

(*) Required fields.

Attention: Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. For all other comments, please send your remarks via contact us. Only comments written in English can be processed.

Captcha image
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.