01
Diseases
Fanconi Anemia, Complementation Group A (Disorder)
fanconi anemia, complementation group a (disorder)
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 8
Basic Information
Grouped by core information, identifiers, and descriptions.
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Core Information
- Disease Name
- Fanconi Anemia, Complementation Group A (Disorder)
- Standard Disease Name
- fanconi anemia, complementation group a (disorder)
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- No data
- OMIM ID
- 227650|607139
- UMLS ID
- C3469521
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_02D:Fanconi anemia caused by mutations of the FANCA gene. FANCA gene mutations are the most common cause of Fanconi anemia. This gene provides instructions for making a protein that is involved in the Fanconi anemia (FA) pathway.