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.
|