Disease #05980 (CILD37 (dyskinesia, ciliary, primary, type 37 (CILD37)), OMIM:617577)
| Official abbreviation |
CILD37 |
| Name |
dyskinesia, ciliary, primary, type 37 (CILD37) |
| OMIM ID |
617577 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
DNAH1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-10-22 15:38:23 +02:00 (CEST) |
| Date last edited |
N/A |
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