Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the face (HP:0000271)help
Parent Node:
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Facial cleft (HP:0002006)help
..Starting node
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Paramedian facial cleft (HP:0031571)help
Term ID: 31571
Name: Paramedian facial cleft
Synonym:
Definition: A type of facial cleft located near to but not directly on the midline of the face.
Comments:
Reference: HP:0031571
Genes and Diseases:
 
       Child Nodes:
........expandTessier number 1 facial cleft (HP:0031572) help
........expandTessier number 2 facial cleft (HP:0031573) help
........expandTessier number 12 facial cleft (HP:0031584) help
........expandTessier number 13 facial cleft (HP:0031585) help

 Sister Nodes: 
..expandMidline facial cleft (HP:0100629) help
..expandOrbital cleft (HP:0031574) help
..expandTransverse facial cleft (HP:0100731) 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:0031571HP:0031571Paramedian facial cleft0ALX4 CL E G H60529450OMIM:613451Frontonasal dysplasia 2132
HP:0031571HP:0031584Tessier number 12 facial cleft1 CL E G H
HP:0031571HP:0031573Tessier number 2 facial cleft1 CL E G H
HP:0031571HP:0031572Tessier number 1 facial cleft1 CL E G H
HP:0031571HP:0031585Tessier number 13 facial cleft1ALX4 CL E G H60529450OMIM:613451Frontonasal dysplasia 2132


Genes (1) :ALX4

Diseases (1) :OMIM:613451
 

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