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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Abnormal blistering of the skin +   
Abnormal cutaneous collagen fibril morphology +   
Abnormal cutaneous elastic fiber morphology +   
Abnormal dermis morphology +   
Abnormal dermoepidermal junction morphology +   
Abnormal elasticity of skin +   
Abnormal epidermal morphology +   
Abnormal fetal skin morphology +   
Abnormality of skin pigmentation +   
Cutaneous wound +   
Decreased skin turgor 
Dermal immune complex deposition 
Dermal translucency  
Dry skin  
Flaky paint dermatosis 
Generalized abnormality of skin +   
Keratosis pilaris  
Lichenification +   
Localized skin lesion +   
Maceration  
Ochronosis  
Brown or blue-gray discoloration of the skin that can present on the axillary and inguinal areas, face, palms or soles. In addition, blue-black discoloration can be apparent on skin overlying cartilage in which the pigment is deposited, such as the ears. This is a characteristic manifestation of alkaptonuria, which is an autosomal recessively inherited deficiency of homogentisic acid oxidase that results in accumulation of homogentisic acid in collagenous structures. The sclerae are also typically involved.
Pallor +   
Pigment incontinence  
Poikiloderma +   
Regional abnormality of skin +   
Skin infectious agent +  
Stiff skin  
Thickened skin +   
Tonofilament clumping  

Synonyms
Exact Synonyms: Ochronotic arthritis
Xrefs: SNOMEDCT_US:410042009 ;   UMLS:C0028817
Definition Sources: https://orcid.org/0000-0002-0736-9199, PMID:24447956, PMID:26929770

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