Human Phenotype Ontology 
Grandparent Node:
expandLocalized skin lesion (HP:0011355)help
Parent Node:
expandNevus (HP:0003764)help
..Starting node
..expandNevus of Ota (HP:0009920)help
Term ID: 9920
Name: Nevus of Ota
Synonym: Congenital melanosis bulbi; Naevus fuscoceruleus ophthalmomaxillaris; Nevus fuscoceruleus ophthalmomaxillaris; Oculodermal melanocytosis
Definition: A dermal melanocytic hamartoma that presents as bluish hyperpigmentation on the face along the first or second branches of the trigeminal nerve. Nevus of Ota may involve the sclera.
Comments:
Reference: HP:0009920
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAtypical nevi in non-sun exposed areas (HP:0001074) help
..expandAtypical nevus (HP:0001062) help
..expandBlue nevus (HP:0100814) help
..expandCongenital panfollicular nevus (HP:0025471) help
..expandConnective tissue nevi (HP:0100898) help
..expandEpidermal nevus (HP:0010816) help
..expandMelanocytic nevus (HP:0000995) help
..expandNevus flammeus (HP:0001052) help
..expandNevus sebaceus (HP:0025511) help
..expandNevus spilus (HP:0025510) help
..expandNumerous nevi (HP:0001054) 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:0009920HP:0009920Nevus of Ota0 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.