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:
Generalized abnormality of skin (HP:0011354)

Parent Node:
Cutaneous photosensitivity (HP:0000992)

..Starting node
..Early cutaneous photosensitivity (HP:0007396)

Term ID:

7396

Name:

Early cutaneous photosensitivity

Synonym:

Sun sensitivity occurring early in life

Definition:

Photosensitivity of the skin occurring early in life.

Comments:

Reference:

HP:0007396

Genes and Diseases:

Child Nodes:

Sister Nodes:

Severe photosensitivity (HP:0007537)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0007396	HP:0007396	Early cutaneous photosensitivity	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.