Disease #00061

Official abbreviation FANCA
Name Fanconi anemia, complementation group A
OMIM ID 227650
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene FANCA
Associated tissues -
Disease features -
Remarks -


Individuals

1 entry on 1 page. Showing entry 1.
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00020868 - F Al Bara, Syria - Syrian no - FANCA - - BRCA2, FANCA, FANCD2, PALB2, RECQL4, SLX4, TSC2 11 1 Despoina Kalfakakou
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