Disease #00125 (FANCA (Fanconi anemia, complementation group A (FANCA)), OMIM:227650)
Official abbreviation |
FANCA |
Name |
Fanconi anemia, complementation group A (FANCA) |
OMIM ID |
227650 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
1021 |
Phenotype entries for this disease |
992 |
Associated with 1 gene |
FANCA |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2013-05-03 13:49:20 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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