Human Phenotype Ontology 
Grandparent Node:
expandobsolete Abnormality of calvarial morphology (HP:0002648)help
Parent Node:
expandPlagiocephaly (HP:0001357)help
..Starting node
..expandAnterior plagiocephaly (HP:0011326)help
Term ID: 11326
Name: Anterior plagiocephaly
Synonym: Anterior flat head syndrome; Coronal synostosis; Deformational anterior plagiocephaly; Deformational frontal plagiocephaly; Frontal plagiocephaly; Positional anterior plagiocephaly; Positional frontal plagiocephaly; Unicoronal craniosynostosis
Definition: Asymmetry of the anterior part of the skull.
Comments:
Reference: HP:0011326
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandPosterior plagiocephaly (HP:0011327) 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:0011326HP:0011326Anterior plagiocephaly0ALX4 CL E G H60529450OMIM:613451Frontonasal dysplasia 2132
HP:0011326HP:0011326Anterior plagiocephaly0ATP6V1B2 CL E G H526854ORPHA:79500DOORS syndromeHP:0040284 - Very rare5
HP:0011326HP:0011326Anterior plagiocephaly0PIGO CL E G H8472023215OMIM:614749Hyperphosphatasia with mental retardation syndrome 284
HP:0011326HP:0011326Anterior plagiocephaly0TBC1D24 CL E G H5746529203ORPHA:79500DOORS syndromeHP:0040284 - Very rare271
HP:0011326HP:0011326Anterior plagiocephaly0TCF12 CL E G H693811623OMIM:619718HYPOGONADOTROPIC HYPOGONADISM 26 WITH OR WITHOUT ANOSMIA; HH2628


Genes (5) :ALX4 ATP6V1B2 PIGO TBC1D24 TCF12

Diseases (4) :OMIM:613451 ORPHA:79500 OMIM:614749 OMIM:619718
 

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