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Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Intellectual deficit, X-linked, Snyder type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency
Intellectual deficit, X-linked, Snyder type

LDHA
(UniProt - OMIM)
 SMS
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
LDHA
(0.63)
SMS


Citations in the biomedical literature:


Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency
LDHA
Intellectual deficit, X-linked, Snyder type
SMS



Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency
Intellectual deficit, X-linked, Snyder 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
Synonym(s):
- Snyder-Robinson syndrome
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: x-linked recessive
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.