Disease #01365 (HSCR-1 (Hirschsprung disease, type 1 (HSCR-1)), OMIM:142623)

Official abbreviation HSCR-1
Name Hirschsprung disease, type 1 (HSCR-1)
OMIM ID 142623
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene RET
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A