Disease #02292 (HSCR2 (Hirschsprung disease, susceptibility to, type 2 (HSCR-2)), OMIM:600155)

Official abbreviation HSCR2
Name Hirschsprung disease, susceptibility to, type 2 (HSCR-2)
OMIM ID 600155
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene EDNRB
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00089039 - - - - - Germany - - - - - HSCR2 - EDNRB EDNRB 1 1 Gemeinschaftspraxis für Humangenetik Dresden
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