Atrophic scars

Symptom Information:

Symptom ID: HPO:0001075
Synonyms:
Thin, atrophic scars [HPO:0001075]
Atrophic scar [HPO:0001075]
Atrophic scars [OMIM:Atrophic scars]
Thin, atrophic scars [OMIM:Thin, atrophic scars]
Atrophic scars (rare) [OMIM:Atrophic scars (rare)]
Quality:
Cross references:
OMIM: "Atrophic scars" [OMIM:Atrophic scars]
OMIM: "Thin, atrophic scars" [OMIM:Thin, atrophic scars]
OMIM: "Atrophic scars (rare)" [OMIM:Atrophic scars (rare)]
Is a (Direct Parents):
HPO         Dermal atrophy
HPO         Atypical scarring of skin
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of connective tissue(HPO:0003549)
          Scarring(HPO:0100699)
             Atypical scarring of skin(HPO:0000987)
                Atrophic scars(HPO:0001075)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Generalized abnormality of skin(HPO:0011354)
                Atypical scarring of skin(HPO:0000987)
                   Atrophic scars(HPO:0001075)
             Localized skin lesion(HPO:0011355)
                Aplasia/Hypoplasia of the skin(HPO:0008065)
                   Dermal atrophy(HPO:0004334)
                      Atrophic scars(HPO:0001075)
MedDRA:
Database Frequency: 15 / 7739
Resource:

All diseases associated with this symptom:

EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 1 (OMIM:130070)
EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 2 (OMIM:615425)
Ehlers-Danlos syndrome type 7A (Orphanet:99875)
Ehlers-Danlos syndrome type 7B (Orphanet:99876)
Ehlers-Danlos syndrome, arthrochalasic type (Orphanet:1899)
Ehlers-Danlos syndrome, cardiac valvular type (Orphanet:230851)
Ehlers-Danlos syndrome, progeroid type (Orphanet:75496)
Epidermolysis bullosa simplex, Dowling-Meara type (Orphanet:79396)
Generalized dominant dystrophic epidermolysis bullosa (Orphanet:231568)
Junctional epidermolysis bullosa - pyloric atresia (Orphanet:79403)
Junctional epidermolysis bullosa, Herlitz type (Orphanet:79404)
LOEYS-DIETZ SYNDROME, TYPE 2A (OMIM:608967)
Marfan syndrome type 2 (Orphanet:284973)
Severe generalized recessive dystrophic epidermolysis bullosa (Orphanet:79408)
Transient bullous dermolysis of the newborn (Orphanet:79411)