Disease #04524 (MMDS4 (mitochondrial dysfunctions, multiple, syndrome, type 4), OMIM:616370)
| Official abbreviation |
MMDS4 |
| Name |
mitochondrial dysfunctions, multiple, syndrome, type 4 |
| OMIM ID |
616370 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
ISCA2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
| Date last edited |
2024-11-25 09:59:53 +01:00 (CET) |
Individuals
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