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:
Abnormality of the outer ear (HP:0000356)

Grandparent Node:
Neoplasm of the ear (HP:0012780)

Parent Node:
Basal cell carcinoma (HP:0002671)

Parent Node:
Neoplasm of the outer ear (HP:0040095)

..Starting node
..Basalioma of the outer ear (HP:0040098)

Term ID:

40098

Name:

Basalioma of the outer ear

Synonym:

Definition:

Comments:

Reference:

HP:0040098

Genes and Diseases:

Child Nodes:

Sister Nodes:

Exostosis of the external auditory canal (HP:0004459)

Neoplasm of the ceruminal gland (HP:0040097)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0040098	HP:0040098	Basalioma of the outer ear	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.