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.
Legend  

AscendingIndividual ID     

Reference     

Gender     

Geographic origin     

Geographic origin     

Population     

Consanguinity     

Remarks     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00020868 - F Al Bara, Syria - Syrian no - FANCA - - BRCA2, FANCA, FANCD2, PALB2, RECQL4, SLX4, TSC2 10 1 Despoina Kalfakakou
Legend