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Autosomal dominant intermediate Charcot-Marie-Tooth disease type D
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain
1 associated gene
No signs/symptoms info
Autosomal dominant intermediate Charcot-Marie-Tooth disease type D
Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain

MPZ
(UniProt - OMIM)
 MPZ
(UniProt - OMIM)

COMMON
GENES 		MPZ


Citations in the biomedical literature:


Autosomal dominant intermediate Charcot-Marie-Tooth disease type D
MPZ
Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain



Autosomal dominant intermediate Charcot-Marie-Tooth disease type D
Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain

Synonym(s):
- CMTDID
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.