Human Phenotype Ontology 
Grandparent Node:
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Abnormal aggressive, impulsive or violent behavior (HP:0006919)help
Parent Node:
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Self-injurious behavior (HP:0100716)help
..Starting node
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Skin-picking (HP:0012166)help
Term ID: 12166
Name: Skin-picking
Synonym: Compulsive skin picking; Dermatillomania
Definition: Repetitive and compulsive picking of skin which results in tissue damage.
Comments:
Reference: HP:0012166
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandHair-pulling (HP:0012167) help
..expandHead-banging (HP:0012168) help
..expandSelf-biting (HP:0012169) help
..expandSelf-mutilation (HP:0000742) 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:0012166HP:0012166Skin-picking0CHD5 CL E G H2603816816OMIM:619873
HP:0012166HP:0012166Skin-picking0CNTNAP2 CL E G H2604713830ORPHA:163681CNTNAP2-related developmental and epileptic encephalopathy518
HP:0012166HP:0012166Skin-picking0HTR2A CL E G H33565293OMIM:164230Obsessive-Compulsive disorder 14
HP:0012166HP:0012166Skin-picking0KMT2E CL E G H5590418541OMIM:618512O'donnell-Luria-Rodan syndrome.1
HP:0012166HP:0012166Skin-picking0MAGEL2 CL E G H545516814ORPHA:398069MAGEL2-related Prader-Willi-like syndromeHP:0040282 - Frequent63
HP:0012166HP:0012166Skin-picking0MAGEL2 CL E G H545516814ORPHA:98754Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15HP:0040283 - Occasional63
HP:0012166HP:0012166Skin-picking0MAGEL2 CL E G H545516814ORPHA:177901Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1HP:0040282 - Frequent63
HP:0012166HP:0012166Skin-picking0MAGEL2 CL E G H545516814ORPHA:177904Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2HP:0040282 - Frequent63
HP:0012166HP:0012166Skin-picking0MAGEL2 CL E G H545516814OMIM:615547Schaaf-Yang syndrome63
HP:0012166HP:0012166Skin-picking0NDN CL E G H46927675ORPHA:98754Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15HP:0040283 - Occasional
HP:0012166HP:0012166Skin-picking0NDN CL E G H46927675ORPHA:177901Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1HP:0040282 - Frequent
HP:0012166HP:0012166Skin-picking0NDN CL E G H46927675ORPHA:177904Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2HP:0040282 - Frequent
HP:0012166HP:0012166Skin-picking0OCA2 CL E G H49488101ORPHA:98754Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15HP:0040283 - Occasional121
HP:0012166HP:0012166Skin-picking0OCA2 CL E G H49488101ORPHA:177901Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1HP:0040282 - Frequent121
HP:0012166HP:0012166Skin-picking0OCA2 CL E G H49488101ORPHA:177904Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2HP:0040282 - Frequent121
HP:0012166HP:0012166Skin-picking0SIM1 CL E G H649210882ORPHA:398079SIM1-related Prader-Willi-like syndromeHP:0040282 - Frequent40
HP:0012166HP:0012166Skin-picking0SLC6A4 CL E G H653211050OMIM:164230Obsessive-Compulsive disorder 152
HP:0012166HP:0012166Skin-picking0SNRPN CL E G H663811164ORPHA:98754Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15HP:0040283 - Occasional37
HP:0012166HP:0012166Skin-picking0SNRPN CL E G H663811164ORPHA:177901Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1HP:0040282 - Frequent37
HP:0012166HP:0012166Skin-picking0SNRPN CL E G H663811164ORPHA:177904Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2HP:0040282 - Frequent37
HP:0012166HP:0012166Skin-picking0SNRPN CL E G H663811164ORPHA:177907Prader-Willi syndrome due to translocationHP:0040283 - Occasional37
HP:0012166HP:0012166Skin-picking0USP7 CL E G H787412630ORPHA:50005516p13.2 microdeletion syndromeHP:0040283 - Occasional2


Genes (11) :CHD5 CNTNAP2 HTR2A KMT2E MAGEL2 NDN OCA2 SIM1 SLC6A4 SNRPN USP7

Diseases (12) :OMIM:619873 ORPHA:163681 OMIM:164230 OMIM:618512 ORPHA:398069 ORPHA:98754 ORPHA:177901 ORPHA:177904 OMIM:615547 ORPHA:398079 ORPHA:177907 ORPHA:500055
 

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