Human Phenotype Ontology 
Grandparent Node:
expandAbnormal bone structure (HP:0003330)help
Parent Node:
expandAbnormal bone ossification (HP:0011849)help
..Starting node
..expandAbnormal intramembranous ossification (HP:0012790)help
Term ID: 12790
Name: Abnormal intramembranous ossification
Synonym: Abnormal intramembranous bone ossification
Definition: An anomaly in the process of intramembranous ossification by which flat bones (cranial bones of the skull, i.e., the frontal, parietal, occipital, and temporal bones, and the clavicles) are formed.
Comments:
Reference: HP:0012790
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal enchondral ossification (HP:0003336) help
..expandAbnormality of bone mineral density (HP:0004348) help
..expandDecreased skull ossification (HP:0004331) help
..expandEctopic ossification (HP:0011986) 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:0012790HP:0012790Abnormal intramembranous ossification0 CL E G H


Genes (0) :

Diseases (0) :
 

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