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Navajo neurohepatopathy
1 OMIM reference -
1 associated gene
9 connected diseases
No signs/symptoms info
Disease Type of connection
Isolated NADH-CoQ reductase deficiency
Leigh syndrome with leukodystrophy
Combined oxidative phosphorylation defect type 2
Giant cell glioblastoma
Gliosarcoma
Infantile Refsum disease
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency
Neonatal adrenoleukodystrophy
Zellweger syndrome
Synonym(s):
- Navajo neuropathy
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
MPV17 P39210137960
No signs/symptoms info available.