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Pelizaeus-Merzbacher disease, connatal form
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Pelizaeus-Merzbacher disease in female carriers
1 associated gene
No signs/symptoms info
Pelizaeus-Merzbacher disease, connatal form
Pelizaeus-Merzbacher disease in female carriers

PLP1
(UniProt - OMIM)
 PLP1
(UniProt - OMIM)

COMMON
GENES 		PLP1


Citations in the biomedical literature:


Pelizaeus-Merzbacher disease, connatal form
PLP1
Pelizaeus-Merzbacher disease in female carriers



Pelizaeus-Merzbacher disease, connatal form
Pelizaeus-Merzbacher disease in female carriers

Synonym(s):
- Connatal PMD
- Pelizaeus-Merzbacher disease type II
- Severe PMD
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: any age
Type of inheritance: x-linked recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: normal
Type of inheritance: x-linked recessive
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.