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Intellectual deficit, X-linked, Turner type
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary motor and sensory neuropathy type 5
1 OMIM reference -
1 associated gene
No signs/symptoms info
Intellectual deficit, X-linked, Turner type
Hereditary motor and sensory neuropathy type 5

HUWE1
(UniProt - OMIM)
 MFN2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
HUWE1
(0.63)
MFN2


Citations in the biomedical literature:


Intellectual deficit, X-linked, Turner type
HUWE1
Hereditary motor and sensory neuropathy type 5
MFN2



Intellectual deficit, X-linked, Turner type
Hereditary motor and sensory neuropathy type 5

Synonym(s):
(no synonyms)

Synonym(s):
- Charcot-Marie-Tooth disease - pyramidal features
- HMSN 5
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: x-linked dominant
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.