Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the liver (HP:0001392)help
Grandparent Node:
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Neoplasm of the gastrointestinal tract (HP:0007378)help
Parent Node:
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Hemangioma (HP:0001028)help
Parent Node:
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Neoplasm of the liver (HP:0002896)help
..Starting node
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Hepatic hemangioma (HP:0031207)help
Term ID: 31207
Name: Hepatic hemangioma
Synonym: Hemangioma of the liver; Liver hemangioma
Definition: A congenital vascular malformation in the liver composed of masses of blood vessels that are atypical or irregular in arrangement and size.
Comments:
Reference: HP:0031207
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandHepatoblastoma (HP:0002884) help
..expandHepatocellular adenoma (HP:0012028) help
..expandHepatocellular carcinoma (HP:0001402) 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:0031207HP:0031207Hepatic hemangioma0CCND1 CL E G H5951582OMIM:193300Von hippel-lindau syndrome1
HP:0031207HP:0031207Hepatic hemangioma0CREBBP CL E G H13872348OMIM:180849Rubinstein-Taybi syndrome 1291
HP:0031207HP:0031207Hepatic hemangioma0EP300 CL E G H20333373OMIM:180849Rubinstein-Taybi syndrome 1250
HP:0031207HP:0031207Hepatic hemangioma0VHL CL E G H742812687OMIM:193300Von hippel-lindau syndrome490


Genes (4) :CCND1 CREBBP EP300 VHL

Diseases (2) :OMIM:193300 OMIM:180849
 

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