Human Phenotype Ontology 
Grandparent Node:
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Localized skin lesion (HP:0011355)help
Parent Node:
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Capillary malformation (HP:0025104)help
..Starting node
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Nevus anemicus (HP:0025105)help
Term ID: 25105
Name: Nevus anemicus
Synonym: Naevus anaemicus
Definition: A congenital skin lesion characterized by irregular hypopigmented macules that coalesce to form plaques and occur particularly on the chest. It is generally present at birth or develops in the first days of life. It is more common in females. Diagnosis is confirmed by applying gentle friction to the lesion and the surrounding skin and checking that the erythema produced in the healthy skin does not appear in the hypopigmented lesion. This pale macule becomes more conspicuous when the lesion and its surroundings are rubbed. The margin of the naevus is ill-defined and consists of an archipelago of small anaemic spots.
Comments:
Reference: HP:0025105
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAngioma serpentinum (HP:0025108) help
..expandCutis marmorata telangiectatica congenita (HP:0025107) help
..expandNevus flammeus (HP:0001052) help
..expandNevus roseus (HP:0025106) 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:0025105HP:0025105Nevus anemicus0NF1 CL E G H47637765ORPHA:9768517q11 microdeletion syndromeHP:0040282 - Frequent1952


Genes (1) :NF1

Diseases (1) :ORPHA:97685
 

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