Human Phenotype Ontology 
Grandparent Node:
expandAbnormal skull morphology (HP:0000929)help
Parent Node:
expandAbnormal facial skeleton morphology (HP:0011821)help
..Starting node
..expandFrontomalar faciosynostosis (HP:0430004)help
Term ID: 430004
Name: Frontomalar faciosynostosis
Synonym:
Definition:
Comments:
Reference: HP:0430004
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal ethmoid bone morphology (HP:0430005) help
..expandAbnormal frontal bone morphology (HP:0430000) help
..expandAbnormal jaw morphology (HP:0030791) help
..expandAbnormal lacrimal bone morphology (HP:0430002) help
..expandAbnormal palatine bone morphology (HP:0430003) help
..expandAbnormal paranasal sinus morphology (HP:0000245) help
..expandAbnormal vomer morphology (HP:0410000) help
..expandAbnormal zygomatic bone morphology (HP:0010668) help
..expandAplasia of facial bones (HP:0040008) help
..expandCraniofacial asymmetry (HP:0004484) help
..expandCraniofacial hyperostosis (HP:0004493) help
..expandCraniofacial osteosclerosis (HP:0005464) help
..expandHypoplastic facial bones (HP:0002692) 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:0430004HP:0430004Frontomalar faciosynostosis0 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.