Human Phenotype Ontology 
Grandparent Node:
expandFacial cleft (HP:0002006)help
Parent Node:
expandOrbital cleft (HP:0031574)help
..Starting node
..expandTessier number 9 facial cleft (HP:0031581)help
Term ID: 31581
Name: Tessier number 9 facial cleft
Synonym:
Definition: This is an upper lateral orbital cleft. The soft tissue deformity is in the lateral one-third of the upper eyelid, and the bony cleft is through the superolateral orbital angle. Microphthalmia is present. The superolateral bony deficiency of the orbits allows a lateral displacement of the globes. The lateral one-third of the upper eyelid and the outer canthus are distorted, thus preventing apposition to the globe. The upper eyelid does not have a true cleft. A soft tissue furrow radiates superiorly and posterisphenoid is symmetric and normal. Mild cranial base asymmetry is reflected in the pterygoid plates. The left pair is more laterally displaced from the midline. Skull vault plagiocephaly is evident with an apparent reduction in the anteroposterior dimension of the anterior cranial fossa.
Comments:
Reference: HP:0031581
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandTessier number 10 facial cleft (HP:0031582) help
..expandTessier number 11 facial cleft (HP:0031583) help
..expandTessier number 3 facial cleft (HP:0031575) help
..expandTessier number 4 facial cleft (HP:0031576) help
..expandTessier number 5 facial cleft (HP:0031577) 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:0031581HP:0031581Tessier number 9 facial cleft0 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.