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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
7 OMIM references -
12 associated genes
No signs/symptoms info
Glycogen storage disease due to aldolase A deficiency
Hereditary nonpolyposis colon cancer

ALDOA BMPR1A
EPCAM
KRAS
LRRFIP2
MLH1
MLH3
MSH2
MSH6
PIK3CA
PMS1
PMS2
TGFBR2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ALDOA
(0.63)
MLH1



Citations in the biomedical literature:


Glycogen storage disease due to aldolase A deficiency
ALDOA
Hereditary nonpolyposis colon cancer
BMPR1A EPCAM KRAS LRRFIP2 MLH1 MLH3
MSH2 MSH6 PIK3CA PMS1 PMS2 TGFBR2



Glycogen storage disease due to aldolase A deficiency
Hereditary nonpolyposis colon cancer

Synonym(s):
- GSD due to aldolase A deficiency
- GSD type 12
- Glycogen storage disease type 12
- Glycogenosis due to aldolase A deficiency
- Glycogenosis type 12

Synonym(s):
- Familial nonpolyposis colon cancer
- Familial nonpolyposis colorectal cancer
- HNPCC
- Hereditary nonpolyposis colorectal cancer
- Lynch syndrome

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
(no data available)

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
7 OMIM references -
1 MeSH reference: D003123

No signs/symptoms info available.