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

PLP1 PLP1


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.