Disease #06724 (NMOAS (Neuromuscular disease and ocular or auditory anomalies with or without seizures), OMIM:618733)
| Official abbreviation |
NMOAS |
| Name |
Neuromuscular disease and ocular or auditory anomalies with or without seizures |
| OMIM ID |
618733 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
DHX16 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
|