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Adrenomyeloneuropathy
1 OMIM reference -
1 associated gene
8 connected diseases
No signs/symptoms info
Disease Type of connection
CADDS
X-linked cerebral adrenoleukodystrophy
Infantile Refsum disease
Neonatal adrenoleukodystrophy
Zellweger syndrome
B-cell chronic lymphocytic leukemia
Familial isolated congenital asplenia
Rhizomelic chondrodysplasia punctata type 3
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Inborn errors of metabolism
- Rare endocrine disease
- Rare genetic disease
- Rare infertility
- Rare neurologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: -
Average age onset: adulthood
Average age of death: -
Type of inheritance: x-linked recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
ABCD1 P33897300371
No signs/symptoms info available.