Human Phenotype Ontology 
Grandparent Node:
expandAbnormal calvaria morphology (HP:0002683)help
Grandparent Node:
expandHyperostosis (HP:0100774)help
Parent Node:
expandCranial hyperostosis (HP:0004437)help
..Starting node
..expandHyperostosis cranialis interna (HP:0005890)help
Term ID: 5890
Name: Hyperostosis cranialis interna
Synonym: Enlargement of the inner surface of the skull bones; Excessive growth of inner surface of the skull bones; Hyperostosis of the internal surface of the cranial bone; Hyperostosis of the internal surface of the cranial bones; Hypertrophy of the internal surface of the cranial bones; Increased ossification of the internal surface of the cranial bones; Overgrowth of the inner surface of the skull bones; Overgrowth of the inside of the skull; Thick inner surface of the skull bones; Thick internal surface of the cranial bones
Definition: Bony overgrowth of the internal (endosteal) surface of the calvaria and the base of skull.
Comments:
Reference: HP:0005890
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCalvarial hyperostosis (HP:0004490) help
..expandCraniofacial hyperostosis (HP:0004493) help
..expandHyperostosis frontalis interna (HP:0004438) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0005890HP:0005890Hyperostosis cranialis interna0SLC39A14 CL E G H2351620858OMIM:144755Hyperostosis cranialis interna.5
HP:0005890HP:0005890Hyperostosis cranialis interna0TBXAS1 CL E G H691611609OMIM:231095Ghosal hematodiaphyseal dysplasia16


Genes (2) :SLC39A14 TBXAS1

Diseases (2) :OMIM:144755 OMIM:231095
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.