Disease #03316 (MNMN (mononeuropathy of the median nerve, mild (MNMN)), OMIM:613353)

Official abbreviation MNMN
Name mononeuropathy of the median nerve, mild (MNMN)
OMIM ID 613353
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene SH3TC2
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)

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