Human Phenotype Ontology 
Grandparent Node:
expandLocalized skin lesion (HP:0011355)help
Grandparent Node:
expandScarring (HP:0100699)help
Parent Node:
expandAbnormality of facial soft tissue (HP:0011799)help
Parent Node:
expandAtypical scarring of skin (HP:0000987)help
..Starting node
..expandAtrophodermia vermiculata (HP:0100837)help
Term ID: 100837
Name: Atrophodermia vermiculata
Synonym: Vermiculata atrophoderma
Definition: Symmetrical vermiform facial atrophy that affects mainly the forehead, the chin, the ear lobes and helices. Atrophodermia vermiculata is characterized by erythema and follicular plugs on the cheeks, developing into painless reticular impressions.
Comments:
Reference: HP:0100837
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAtrophic scars (HP:0001075) help
..expandKeloids (HP:0010562) help
..expandScarring alopecia of scalp (HP:0004552) 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:0100837HP:0100837Atrophodermia vermiculata0NLRP1 CL E G H2286114374OMIM:618803RESPIRATORY PAPILLOMATOSIS, JUVENILE RECURRENT, CONGENITAL; JRRP37


Genes (1) :NLRP1

Diseases (1) :OMIM:618803
 

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