Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the orbital region (HP:0000315)help
Parent Node:
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Abnormal ocular adnexa morphology (HP:0030669)help
..Starting node
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Abnormal common tendinous ring morphology (HP:0030671)help
Term ID: 30671
Name: Abnormal common tendinous ring morphology
Synonym: Abnormality of the common tendinous ring
Definition: Any anomaly of the ring of fibrous tissue that surrounds the optic nerve at its entrance at the apex of the orbit. The common tendinous ring, also known as the annulus of Zinn or annular tendon, is the origin for five of the seven extraocular muscles.
Comments:
Reference: HP:0030671
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal conjunctiva morphology (HP:0000502) help
..expandAbnormal eyebrow morphology (HP:0000534) help
..expandAbnormal eyelid morphology (HP:0000492) help
..expandAbnormal nasolacrimal system morphology (HP:0000614) help
..expandAbnormality of the extraocular muscles (HP:0008049) 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:0030671HP:0030671Abnormal common tendinous ring 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.