Disease #03397 (MCOPCB6 (microphthalmia, isolated, with coloboma, type 6 (MCOPCB6)), OMIM:613703)

Official abbreviation MCOPCB6
Name microphthalmia, isolated, with coloboma, type 6 (MCOPCB6)
OMIM ID 613703
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Digenic dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 2 genes GDF3, GDF6
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-01-28 13:49:58 +01:00 (CET)

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