Human Phenotype Ontology 
Grandparent Node:
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Abnormal retinal morphology (HP:0000479)help
Grandparent Node:
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Hamartoma of the eye (HP:0010568)help
Parent Node:
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Retinal hamartoma (HP:0009594)help
..Starting node
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Retinal racemose hemangioma (HP:0030509)help
Term ID: 30509
Name: Retinal racemose hemangioma
Synonym: Retinal racemose haemangioma
Definition:
Comments:
Reference: HP:0030509
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCombined hamartoma of the retinal pigment epithelium and retina (HP:0030510) help
..expandRetinal astrocytic hamartoma (HP:0012778) help
..expandRetinal capillary hemangioma (HP:0009711) help
..expandRetinal cavernous hemangioma (HP:0030508) 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:0030509HP:0030509Retinal racemose hemangioma0 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.