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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Charcot-Marie-Tooth disease type 4D
Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency

NDRG1 LDHA


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
NDRG1
(0.83)
LDHA



Citations in the biomedical literature:


Charcot-Marie-Tooth disease type 4D
NDRG1
Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency
LDHA



Charcot-Marie-Tooth disease type 4D
Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency

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

Synonym(s):
- GSD due to lactate dehydrogenase M-subunit deficiency
- GSD type 11
- Glycogen storage disease type 11
- Glycogenosis due to lactate dehydrogenase M-subunit deficiency
- Glycogenosis type 11
- LDH-M subunit deficiency
- Lactate dehydrogenase A deficiency

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic 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:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive

External references:
1 OMIM reference -
1 MeSH reference: C535716
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.