Disease #05522

Official abbreviation HHT-1
Name telangiectasia hemorrhagic, hereditary, type 1 (HHT-1, Osler-Rendu-Weber disease)
OMIM ID -
Individuals reported having this disease 1
Phenotype entries for this disease 0
Associated with 1 gene ENG
Associated tissues -
Disease features autosomal dominant
Remarks -


Individuals

1 entry on 1 page. Showing entry 1.
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00229539 - - - - - - - - 0 - - HHT-1 - ENG ENG 1 1 Gemeinschaftspraxis für Humangenetik Dresden
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