Disease #03401 (HSCR-3 (Hirschsprung disease, type 3 (HSCR-3)), OMIM:613711)

Official abbreviation HSCR-3
Name Hirschsprung disease, type 3 (HSCR-3)
OMIM ID 613711
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene GDNF
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A