Human Phenotype Ontology 
Grandparent Node:
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Phenotypic abnormality (HP:0000118)help
Parent Node:
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Abnormality of the integument (HP:0001574)help
..Starting node
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Abnormality of the skin (HP:0000951)help
Term ID: 951
Name: Abnormality of the skin
Synonym: Abnormality of the skin; dermatopathy; dermopathy; Skin abnormality
Definition: An abnormality of the skin.
Comments:
Reference: HP:0000951
Genes and Diseases:There are 700 terms for your input, too many to show detail here. Please try its child terms.
 
       Child Nodes:
........expandNeoplasm of the skin (HP:0008069) help
................... HP:0001031 Subcutaneous lipoma
................... HP:0001067 Neurofibromas
................... HP:0002671 Basal cell carcinoma
................... HP:0002860 Squamous cell carcinoma
................... HP:0006755 Cutaneous leiomyosarcoma
................... HP:0006769 Myxoid subcutaneous tumors
................... HP:0006773 Cutaneous angiolipomas
................... HP:0007437 Multiple cutaneous leiomyomas
................... HP:0007541 Frontal cutaneous lipoma
................... HP:0007606 Multiple cutaneous malignancies
................... HP:0007620 Cutaneous leiomyoma
................... HP:0009593 Peripheral Schwannoma
................... HP:0009720 Adenoma sebaceum
................... HP:0012035 Steatocystoma multiplex
................... HP:0012056 Cutaneous melanoma
................... HP:0012740 Papilloma
................... HP:0012842 Skin appendage neoplasm
................... HP:0025127 Actinic keratosis
................... HP:0025432 Acanthoma
................... HP:0030428 Cutaneous myxoma
................... HP:0030436 Fibrofolliculoma
................... HP:0030447 Merkel cell skin cancer
................... HP:0031018 Eccrine syringofibroadenoma
................... HP:0031287 Seborrheic keratosis
................... HP:0031525 Keratoacanthoma
................... HP:0031549 Lymphocytoma cutis
................... HP:0100726 Kaposi's sarcoma
................... HP:0200151 Cutaneous mastocytosis
........expandAbnormality of skin morphology (HP:0011121) help
................... HP:0000958 Dry skin
................... HP:0000980 Pallor
................... HP:0001000 Abnormality of skin pigmentation
................... HP:0001029 Poikiloderma
................... HP:0001072 Thickened skin
................... HP:0008066 Abnormal blistering of the skin
................... HP:0010647 Abnormal elasticity of skin
................... HP:0010648 Dermal translucency
................... HP:0011124 Abnormality of epidermal morphology
................... HP:0011354 Generalized abnormality of skin
................... HP:0011355 Localized skin lesion
................... HP:0011356 Regional abnormality of skin
................... HP:0025082 Abnormal cutaneous elastic fiber morphology
................... HP:0025083 Elevated dermal desmosine content
................... HP:0030053 Stiff skin
................... HP:0030764 Ochronosis
................... HP:0031512 Abnormal cutaneous collagen fibril morphology
................... HP:0031538 Abnormal dermoepidermal junction morphology
................... HP:0100725 Lichenification
........expandAbnormality of skin physiology (HP:0011122) help
................... HP:0000989 Pruritus
................... HP:0011123 Inflammatory abnormality of the skin
................... HP:0025531 Harlequin phenomenon
................... HP:0025532 Positive pathergy test
................... HP:0030331 Impaired stimulus-induced skin wrinkling

 Sister Nodes: 
..expandAbnormality of platysma (HP:3000013) help
..expandAbnormality of skin adnexa morphology (HP:0011138) help
..expandAbnormality of skin adnexa physiology (HP:0025276) help


Genes (0) :

Diseases (0) :
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.