Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the face (HP:0000271)help
Parent Node:
expandAbnormality of the periorbital region (HP:0000606)help
..Starting node
..expandBitemporal forceps marks (HP:0011336)help
Term ID: 11336
Name: Bitemporal forceps marks
Synonym: Bitemporal aplasia cutis congenita; Congenital ectodermal dysplasia of the face; Congenital, bilateral, scarlike facial lesions; Focal facial dermal dysplasia; Temporal skin defect
Definition: Bilateral temporal scarlike defects, which are said to resemble forceps marks.
Comments:
Reference: HP:0011336
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal eyebrow morphology (HP:0000534) help
..expandAbnormal morphology of bony orbit of skull (HP:3000030) help
..expandAbnormality of the supraorbital ridges (HP:0100538) help
..expandBitemporal hollowing (HP:0025386) help
..expandInfra-orbital crease (HP:0100876) help
..expandInfra-orbital fold (HP:0011232) help
..expandOrbital cyst (HP:0001144) help
..expandPeriorbital ecchymosis with tarsal plate sparing (HP:0025553) help
..expandPeriorbital edema (HP:0100539) help
..expandPeriorbital fullness (HP:0000629) help
..expandPeriorbital hyperpigmentation (HP:0001106) help
..expandPeriorbital purpura (HP:0025552) help
..expandPeriorbital wrinkles (HP:0000607) 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:0011336HP:0011336Bitemporal forceps marks0CYP26C1 CL E G H34066520577OMIM:614974FOCAL FACIAL DERMAL DYSPLASIA 4; FFDD42
HP:0011336HP:0011336Bitemporal forceps marks0TWIST2 CL E G H11758120670OMIM:227260FOCAL FACIAL DERMAL DYSPLASIA 3, SETLEIS TYPE; FFDD37


Genes (2) :CYP26C1 TWIST2

Diseases (2) :OMIM:614974 OMIM:227260
 

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