Disease #07047 (DIGFAN (developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy), OMIM:619090)

Official abbreviation DIGFAN
Name developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy
OMIM ID 619090
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene MORC2
Associated tissues -
Disease features -
Remarks -
Date created 2023-12-04 21:35:07 +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.