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Null syndrome
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Pelizaeus-Merzbacher disease in female carriers
1 associated gene
No signs/symptoms info
Null syndrome
Pelizaeus-Merzbacher disease in female carriers

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

COMMON
GENES 		PLP1


Citations in the biomedical literature:


Null syndrome
PLP1
Pelizaeus-Merzbacher disease in female carriers



Null syndrome
Pelizaeus-Merzbacher disease in female carriers

Synonym(s):
- PLP1 null syndrome
- Pelizaeus-Merzbacher disease, null syndrome
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: unknown
Average age onset: childhood
Average age of death: adult
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.