Human Phenotype Ontology 
Grandparent Node:
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Abnormal ocular adnexa morphology (HP:0030669)help
Grandparent Node:
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Abnormality of the musculature (HP:0003011)help
Parent Node:
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Abnormality of the extraocular muscles (HP:0008049)help
..Starting node
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Abnormality of lateral rectus extra-ocular muscle (HP:3000069)help
Term ID: 3000069
Name: Abnormality of lateral rectus extra-ocular muscle
Synonym:
Definition: An abnormality of a lateral rectus extra-ocular muscle.
Comments:
Reference: HP:3000069
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal levator palpebrae superioris morphology (HP:3000072) help
..expandAbnormality of inferior oblique extraocular muscle (HP:3000057) help
..expandAbnormality of inferior rectus extraocular muscle (HP:3000058) help
..expandAbsent extraocular muscles (HP:0007886) help
..expandCongenital extraocular muscle anomaly (HP:0007647) help
..expandCongenital fibrosis of extraocular muscles (HP:0001491) help
..expandSuperior rectus atrophy (HP:0012242) 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:3000069HP:3000069Abnormality of lateral rectus extra-ocular muscle0 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.