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 |
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