Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Neoplasm by anatomical site (HP:0011793)

Parent Node:
Soft tissue neoplasm (HP:0031459)

..Starting node
..Benign muscle neoplasm (HP:0031460)

Term ID:

31460

Name:

Benign muscle neoplasm

Synonym:

Definition:

A benign mesenchymal neoplasm arising from smooth, skeletal, or cardiac muscle tissue [NCIT:C4882].

Comments:

Reference:

HP:0031460

Genes and Diseases:

Child Nodes:

........

Intramuscular Myxoma (HP:0031461)

Sister Nodes:

Diffuse leiomyomatosis (HP:0006756)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031460	HP:0031460	Benign muscle neoplasm	0	CL E G H
HP:0031460	HP:0031461	Intramuscular Myxoma	1	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.