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:
Melanoma (HP:0002861)

Grandparent Node:
Neoplasm of the skin (HP:0008069)

Parent Node:
Cutaneous melanoma (HP:0012056)

..Starting node
..Nodular melanoma (HP:0012058)

Term ID:

12058

Name:

Nodular melanoma

Synonym:

Definition:

A type of melanoma that starts as a raised area that is usually dark blackish-blue or bluish-red but may not have any color.

Comments:

Reference:

HP:0012058

Genes and Diseases:

Child Nodes:

Sister Nodes:

Acral lentiginous melanoma (HP:0012060)

Lentigo maligna melanoma (HP:0012059)

Superficial spreading melanoma (HP:0012057)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012058	HP:0012058	Nodular melanoma	0	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.