Human Phenotype Ontology 
Grandparent Node:
expandAbnormal skull morphology (HP:0000929)help
Parent Node:
expandAbnormal calvaria morphology (HP:0002683)help
..Starting node
..expandobsolete Abnormality of calvarial morphology (HP:0002648)help
Term ID: 2648
Name: obsolete Abnormality of calvarial morphology
Synonym:
Definition:
Comments:
Reference: HP:0002648
Genes and Diseases:
 
       Child Nodes:
........expandTrigonocephaly (HP:0000243) help
........expandBrachycephaly (HP:0000248) help
................... HP:0000244 Brachyturricephaly
................... HP:0004487 Acrobrachycephaly
........expandTurricephaly (HP:0000262) help
................... HP:0000244 Brachyturricephaly
................... HP:0000263 Oxycephaly
........expandCranial asymmetry (HP:0000267) help
................... HP:0004484 Craniofacial asymmetry
........expandDolichocephaly (HP:0000268) help
................... HP:0030799 Scaphocephaly
........expandPlagiocephaly (HP:0001357) help
................... HP:0011326 Anterior plagiocephaly
................... HP:0011327 Posterior plagiocephaly
........expandCalvarial skull defect (HP:0001362) help
........expandCraniosynostosis (HP:0001363) help
................... HP:0004440 Coronal craniosynostosis
................... HP:0004442 Sagittal craniosynostosis
................... HP:0004443 Lambdoidal craniosynostosis
................... HP:0005472 Orbital craniosynostosis
................... HP:0011324 Multiple suture craniosynostosis
........expandCloverleaf skull (HP:0002676) help
........expandSkull asymmetry (HP:0002678) help
........expandBroad skull (HP:0002682) help
........expandPlatybasia (HP:0002691) help
........expandAbnormality of the parietal bone (HP:0002696) help
................... HP:0000242 Parietal bossing
................... HP:0002695 Symmetrical, oval parietal bone defects
................... HP:0002697 Parietal foramina
........expandBiparietal narrowing (HP:0004422) help
........expandAbnormal shape of the occiput (HP:0011217) help
................... HP:0000269 Prominent occiput
................... HP:0005469 Flat occiput
........expandAbnormal shape of the frontal region (HP:0011218) help
................... HP:0002007 Frontal bossing
................... HP:0005466 Hypoplasia of the frontal bone
........expandObliteration of the calvarial diploe (HP:0030312) help
........expandAcrania (HP:0030716) help

 Sister Nodes: 
..expandAbnormality of the fontanelles or cranial sutures (HP:0000235) help
..expandCranial hyperostosis (HP:0004437) help
..expandDecreased calvarial ossification (HP:0005474) help
..expandDense calvaria (HP:0000250) help
..expandThickened calvaria (HP:0002684) help
..expandThin calvarium (HP:0010539) 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:0002648HP:0002648obsolete Abnormality of calvarial morphology0 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.