Disease #06776 (INSDM (Insulinomatosis and diabetes mellitus), OMIM:147630)

Official abbreviation INSDM
Name Insulinomatosis and diabetes mellitus
OMIM ID 147630
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene MAFA
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A

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