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Pelizaeus-Merzbacher disease, classic form

1 associated gene
No signs/symptoms info

COMMON GENES: 1

Pelizaeus-Merzbacher disease, connatal form

1 associated gene
No signs/symptoms info

Pelizaeus-Merzbacher disease, classic form

Pelizaeus-Merzbacher disease, connatal form

PLP1

(UniProt - OMIM)

PLP1

(UniProt - OMIM)


COMMON GENES	PLP1

Citations in the biomedical literature:

Pelizaeus-Merzbacher disease, classic form		Pelizaeus-Merzbacher disease, connatal form
	Synonym(s): - classic PMD		Synonym(s): - Connatal PMD - Pelizaeus-Merzbacher disease type II - Severe PMD

	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: 1-9 / 1 000 000 Average age onset: neonatal/infancy Average age of death: adult Type of inheritance: x-linked recessive		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

	External references: No OMIM references No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.