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 |
AD |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
SLC39A14 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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