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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
2 associated genes
No signs/symptoms info
Charcot-Marie-Tooth disease type 4D
Bifunctional enzyme deficiency

NDRG1 EHHADH
HSD17B4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
NDRG1
(0.73)
HSD17B4



Citations in the biomedical literature:


Charcot-Marie-Tooth disease type 4D
NDRG1
Bifunctional enzyme deficiency
EHHADH HSD17B4



Charcot-Marie-Tooth disease type 4D
Bifunctional enzyme deficiency

Synonym(s):
- CMT4D
- HMSN, Lom type
- Hereditary motor and sensory neuropathy, Lom type

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
1 MeSH reference: C535716
External references:
1 OMIM reference -
1 MeSH reference: C536663

No signs/symptoms info available.