Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of skin adnexa morphology (HP:0011138)help
Grandparent Node:
expandNeoplasm of the skin (HP:0008069)help
Parent Node:
expandSkin appendage neoplasm (HP:0012842)help
..Starting node
..expandPoroma (HP:0031405)help
Term ID: 31405
Name: Poroma
Synonym:
Definition: A benign, well circumscribed sweat gland neoplasm with eccrine or apocrine differentiation. It usually presents as a solitary, dome-shaped papule, nodule, or plaque on acral sites. It is characterized by a proliferation of uniform basaloid cells in the dermis and it is associated with the presence of focal ductal and cystic structures [NCIT:C27273].
Comments:
Reference: HP:0031405
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandApocrine hidrocystoma (HP:0031454) help
..expandCylindroma (HP:0031024) help
..expandFollicular infundibulum tumor (HP:0031548) help
..expandHair follicle neoplasm (HP:0012843) help
..expandPilomatrixoma (HP:0030434) help
..expandSebaceous gland carcinoma (HP:0030410) 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:0031405HP:0031405Poroma0WNT10A CL E G H8032613829OMIM:224750Schopf-Schulz-Passarge syndrome.71


Genes (1) :WNT10A

Diseases (1) :OMIM:224750
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.