Human Phenotype Ontology 
Grandparent Node:
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Neoplasm of the peripheral nervous system (HP:0100007)help
Parent Node:
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Abnormal sclera morphology (HP:0000591)help
Parent Node:
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Neoplasm of the eye (HP:0100012)help
Parent Node:
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Schwannoma (HP:0100008)help
..Starting node
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Scleral schwannoma (HP:0100011)help
Term ID: 100011
Name: Scleral schwannoma
Synonym:
Definition:
Comments:
Reference: HP:0100011
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandPeripheral Schwannoma (HP:0009593) help
..expandVestibular Schwannoma (HP:0009588) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100011HP:0100011Scleral schwannoma0 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 June 2019 release.