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 frontalis interna (HP:0004438)help
Term ID: 4438
Name: Hyperostosis frontalis interna
Synonym: Enlargement of the inner surface of the frontal bone; Excessive growth of inner surface of the frontal bone; Hyperostosis of the internal surface of the frontal bone; Hypertrophy of the internal surface of the frontal bone; Increased ossification of the internal surface of the frontal bone; Overgrowth of the inner surface of the frontal bone; Overgrowth of the inside of the frontal bone; Thick inner surface of the frontal bone; Thick internal surface of the frontal bone
Definition: Bony overgrowth of the internal (endosteal) surface of the frontal bone.
Comments:
Reference: HP:0004438
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCalvarial hyperostosis (HP:0004490) help
..expandCraniofacial hyperostosis (HP:0004493) help
..expandHyperostosis cranialis interna (HP:0005890) 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:0004438HP:0004438Hyperostosis frontalis interna0ALMS1 CL E G H7840428ORPHA:64Alström syndromeHP:0040282 - Frequent404
HP:0004438HP:0004438Hyperostosis frontalis interna0ALMS1 CL E G H7840428OMIM:203800Alstrom syndrome.404
HP:0004438HP:0004438Hyperostosis frontalis interna0GNAS CL E G H27784392ORPHA:79443Pseudohypoparathyroidism type 1AHP:0040283 - Occasional101


Genes (2) :ALMS1 GNAS

Diseases (3) :ORPHA:64 OMIM:203800 ORPHA:79443
 

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