Atypical scarring of skin
Symptom Information:
| Symptom ID: | HPO:0000987 | ||||
| Synonyms: |
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| Cross references: |
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| 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) Abnormality of the integument(HPO:0001574) Abnormality of the skin(HPO:0000951) Generalized abnormality of skin(HPO:0011354) Atypical scarring of skin(HPO:0000987) MedDRA: |
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| Database Frequency: | 58 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| ACNE INVERSA, FAMILIAL, 1 | (OMIM:142690) |
| Acquired epidermolysis bullosa | (Orphanet:46487) |
| Autosomal recessive palmoplantar keratoderma and congenital alopecia | (Orphanet:1366) |
| Branchio-oculo-facial syndrome | (Orphanet:1297) |
| Brittle cornea syndrome | (Orphanet:90354) |
| Buschke-Ollendorff syndrome | (Orphanet:1306) |
| COCKAYNE SYNDROME A | (OMIM:216400) |
| COCKAYNE SYNDROME, TYPE III | (OMIM:216411) |
| CREST syndrome | (Orphanet:90290) |
| Cavernous hemangiomas of face - supraumbilical midline raphe | (Orphanet:2124) |
| Cockayne syndrome | (Orphanet:191) |
| Congenital erythropoietic porphyria | (Orphanet:79277) |
| Distal monosomy 19p13.3 | (Orphanet:96129) |
| Dystrophic epidermolysis bullosa | (Orphanet:303) |
| Dystrophic epidermolysis bullosa pruriginosa | (Orphanet:89843) |
| Ehlers-Danlos syndrome type 7A | (Orphanet:99875) |
| Ehlers-Danlos syndrome type 7B | (Orphanet:99876) |
| Ehlers-Danlos syndrome, arthrochalasic type | (Orphanet:1899) |
| Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
| Ehlers-Danlos syndrome, dermatosparaxis type | (Orphanet:1901) |
| Ehlers-Danlos syndrome, fibronectinemic type | (Orphanet:75501) |
| Ehlers-Danlos syndrome, hypermobility type | (Orphanet:285) |
| Ehlers-Danlos syndrome, kyphoscoliotic type | (Orphanet:1900) |
| Ehlers-Danlos syndrome, periodontitis type | (Orphanet:75392) |
| Ehlers-Danlos syndrome, progeroid type | (Orphanet:75496) |
| Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
| Epidermolysis bullosa simplex | (Orphanet:304) |
| Epidermolysis bullosa simplex, Dowling-Meara type | (Orphanet:79396) |
| Familial Dupuytren contracture | (Orphanet:79142) |
| Fetal varicella syndrome | (Orphanet:291) |
| Focal facial dermal dysplasia | (Orphanet:79133) |
| Generalized dominant dystrophic epidermolysis bullosa | (Orphanet:231568) |
| Inherited epidermolysis bullosa | (Orphanet:79361) |
| Kindler syndrome | (Orphanet:2908) |
| Lipoid proteinosis | (Orphanet:530) |
| Loeys-Dietz syndrome type 1 | (Orphanet:60030) |
| Mandibuloacral dysplasia with type B lipodystrophy | (Orphanet:90154) |
| Melorheostosis | (Orphanet:2485) |
| Menkes disease | (Orphanet:565) |
| Mixed connective tissue disease | (Orphanet:809) |
| Mucous membrane pemphigoid | (Orphanet:46486) |
| Occipital horn syndrome | (Orphanet:198) |
| Oculocerebrorenal syndrome | (Orphanet:534) |
| Pemphigus vulgaris | (Orphanet:704) |
| Porphyria cutanea tarda | (Orphanet:101330) |
| Pretibial dystrophic epidermolysis bullosa | (Orphanet:79410) |
| Quinquaud's folliculitis decalvans | (Orphanet:346) |
| Recessive dystrophic epidermolysis bullosa inversa | (Orphanet:79409) |
| Recessive dystrophic epidermolysis bullosa-generalized other | (Orphanet:89842) |
| Retinitis pigmentosa | (Orphanet:791) |
| Retinitis pigmentosa - intellectual deficit - deafness - hypogenitalism | (Orphanet:3085) |
| Rubinstein-Taybi syndrome | (Orphanet:783) |
| Severe generalized recessive dystrophic epidermolysis bullosa | (Orphanet:79408) |
| Systemic sclerosis | (Orphanet:90291) |
| Torticollis - keloids - cryptorchidism - renal dysplasia | (Orphanet:3341) |
| Tricho-oculo-dermo-vertebral syndrome | (Orphanet:3354) |
| Turner syndrome | (Orphanet:881) |
| Ulerythema ophryogenesis | (Orphanet:3406) |