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Autosomal recessive ataxia due to PEX10 deficiency
1 associated gene
6 connected diseases
No signs/symptoms info
Disease Type of connection
Infantile Refsum disease
Neonatal adrenoleukodystrophy
Zellweger syndrome
Idiopathic central precocious puberty
LIG4 syndrome
Omenn syndrome
Synonym(s):
- Mild peroxismal disorder due to PEX10 deficiency
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
PEX10 O60683602859
No signs/symptoms info available.