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
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Individuals

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00288837 family PubMed: Hendrickx 2018, PubMed: Manni 1990 4-generation family, 9 affected (6F, 3M) F;M no Netherlands - - 0 - - HCIN see paper; ... SLC39A14 SLC39A14 1 9 Johan den Dunnen
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