Human Phenotype Ontology 
Grandparent Node:
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Abnormal cornea morphology (HP:0000481)help
Parent Node:
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Abnormal line of Schwalbe morphology (HP:0008048)help
..Starting node
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Abnormally prominent line of Schwalbe (HP:0007873)help
Term ID: 7873
Name: Abnormally prominent line of Schwalbe
Synonym: Prominent Schwalbe lines
Definition:
Comments:
Reference: HP:0007873
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandPosterior embryotoxon (HP:0000627) 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:0007873HP:0007873Abnormally prominent line of Schwalbe0PITX2 CL E G H53089005OMIM:180500Axenfeld-rieger syndrome, type 1.51


Genes (1) :PITX2

Diseases (1) :OMIM:180500
 

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