Disease #05700 (HCIN (hyperostosis cranialis interna (HCIN)), OMIM:144755)
| Official abbreviation |
HCIN |
| Name |
hyperostosis cranialis interna (HCIN) |
| OMIM ID |
144755 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
SLC39A14 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-02-22 10:08:09 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
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