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Ovarioleukodystrophy
1 OMIM reference -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Pseudohypoaldosteronism type 2C
1 OMIM reference -
1 associated gene
No signs/symptoms info
Ovarioleukodystrophy
Pseudohypoaldosteronism type 2C

EIF2B1
(UniProt - OMIM)
 WNK1
(UniProt - OMIM)
EIF2B2
(UniProt - OMIM)
EIF2B3
(UniProt - OMIM)
EIF2B4
(UniProt - OMIM)
EIF2B5
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
EIF2B2
(0.63)
WNK1


Citations in the biomedical literature:


Ovarioleukodystrophy
EIF2B1 EIF2B2 EIF2B3 EIF2B4 EIF2B5
Pseudohypoaldosteronism type 2C
WNK1



Ovarioleukodystrophy
Pseudohypoaldosteronism type 2C

Synonym(s):
(no synonyms)

Synonym(s):
- PHA2C
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare circulatory system disease
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Diseases of the circulatory system -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.