Disease #07031 (MMIHS (megacystis-microcolon-intestinal hypoperistalsis syndrome, type 2), OMIM:619351)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

Official abbreviation	MMIHS
Name	megacystis-microcolon-intestinal hypoperistalsis syndrome, type 2
OMIM ID	619351
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MYH11
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-10-03 16:56:35 +02:00 (CEST)
Date last edited	N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.