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Hemolytic anemia due to diphosphoglycerate mutase deficiency
1 OMIM reference -
1 associated gene
6 connected diseases
No signs/symptoms info
Disease Type of connection
Charcot-Marie-Tooth disease type 1D
Charcot-Marie-Tooth disease type 4E
Cowden syndrome
Dejerine-Sottas syndrome
MODY syndrome
Proteus syndrome
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
BPGM P07738613896
No signs/symptoms info available.