Striae distensae

Symptom Information:

Symptom ID: HPO:0001065
Synonyms:
Purplish striae [HPO:0001065]
Stretch marks [HPO:0001065]
Striae [HPO:0001065]
Striae atrophicae [HPO:0001065]
Striae cutis distensae [HPO:0001065]
Skin striae [HPO:0001065]
Linear atrophy (morphologic abnormality) [Orphanet:23060]
Skin striae (disorder) [Orphanet:23060]
Linear atrophy [Orphanet:23060]
Purplish striae [OMIM:Purplish striae]
Striae [OMIM:Striae]
Striae distensae [OMIM:Striae distensae]
Striae [Orphanet:23060]
Skin striae [Orphanet:23060]
Skin striae [MedDRA:10040925]
Extensive striae [MedDRA:10040925]
Stretch marks [MedDRA:10040925]
Striae [MedDRA:10040925]
Striae atrophic [MedDRA:10040925]
Striae atrophicae [MedDRA:10040925]
Striae purple [MedDRA:10040925]
Striae skin [MedDRA:10040925]
Striae distensae [MedDRA:10040925]
Skin striae [OMIM:Skin striae]
Quality:
Cross references:
Orphanet:23060 "Striae" [Orphanet:23060]
OMIM: "Purplish striae" [OMIM:Purplish striae]
OMIM: "Striae" [OMIM:Striae]
OMIM: "Striae distensae" [OMIM:Striae distensae]
OMIM: "Skin striae" [OMIM:Skin striae]
UMLS:C1963160 "Striae" [HPO:0001065]
UMLS:C0152459 "Linear atrophy" [Orphanet:23060]
Is a (Direct Parents):
HPO         Lack of skin elasticity
HPO         Dermal atrophy
MedDRA Skin hypoplasias and atrophies
Orphanet Abnormality of the skin
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Generalized abnormality of skin(HPO:0011354)
                Abnormality of skin morphology(HPO:0011121)
                   Abnormal elasticity of skin(HPO:0010647)
                      Lack of skin elasticity(HPO:0100679)
                         Striae distensae(HPO:0001065)
             Localized skin lesion(HPO:0011355)
                Aplasia/Hypoplasia of the skin(HPO:0008065)
                   Dermal atrophy(HPO:0004334)
                      Striae distensae(HPO:0001065)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Cornification and dystrophic skin disorders(MedDRA:10011063)
       Skin hypoplasias and atrophies(MedDRA:10040870)
          Striae distensae(HPO:0001065)
Database Frequency: 26 / 7739
Resource:

All diseases associated with this symptom:

ACTH-dependent Cushing syndrome (Orphanet:99892)
ACTH-independent Cushing syndrome (Orphanet:99893)
ACTH-independent macronodular adrenal hyperplasia (Orphanet:189427)
Aneurysm - osteoarthritis syndrome (Orphanet:284984)
Cabezas syndrome (Orphanet:85293)
Carney complex (Orphanet:1359)
Cherubism (Orphanet:184)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
Cushing syndrome due to ectopic ACTH secretion (Orphanet:99889)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Ehlers-Danlos syndrome, fibronectinemic type (Orphanet:75501)
Ehlers-Danlos syndrome, hypermobility type (Orphanet:285)
LOEYS-DIETZ SYNDROME 4 (OMIM:614816)
Loeys-Dietz syndrome type 1 (Orphanet:60030)
MASS SYNDROME (OMIM:604308)
Marfan syndrome (Orphanet:558)
Marfan syndrome type 1 (Orphanet:284963)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1 (OMIM:610489)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2 (OMIM:610475)
Polyvalvular heart disease syndrome (Orphanet:228410)
Primary pigmented nodular adrenocortical disease (Orphanet:189439)
Pruritic urticarial papules and plaques of pregnancy (Orphanet:64745)
Pseudoxanthoma elasticum (Orphanet:758)
STRIAE DISTENSAE, FAMILIAL (OMIM:185200)
Wilson-Turner syndrome (Orphanet:3459)