Dermal atrophy
Symptom Information:
Symptom ID: | HPO:0004334 | ||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||||||||||||||||||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the integument(HPO:0001574) Abnormality of the skin(HPO:0000951) Localized skin lesion(HPO:0011355) Aplasia/Hypoplasia of the skin(HPO:0008065) Dermal atrophy(HPO:0004334) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Cornification and dystrophic skin disorders(MedDRA:10011063) Skin hypoplasias and atrophies(MedDRA:10040870) Dermal atrophy(HPO:0004334) |
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Database Frequency: | 34 / 7739 | ||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ADULT syndrome | (Orphanet:978) |
Acromelanosis | (Orphanet:39) |
Autosomal dominant spastic paraplegia type 3 | (Orphanet:100984) |
Barber-Say syndrome | (Orphanet:1231) |
Branchio-oculo-facial syndrome | (Orphanet:1297) |
COCKAYNE SYNDROME, TYPE III | (OMIM:216411) |
Cockayne syndrome | (Orphanet:191) |
DE SANCTIS-CACCHIONE SYNDROME | (OMIM:278800) |
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1 | (OMIM:127550) |
Dyskeratosis congenita | (Orphanet:1775) |
Dysosteosclerosis | (Orphanet:1782) |
Exostoses - anetodermia - brachydactyly type E | (Orphanet:1962) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
Flynn-Aird syndrome | (Orphanet:2047) |
Focal dermal hypoplasia | (Orphanet:2092) |
Hallermann-Streiff syndrome | (Orphanet:2108) |
Hereditary acrokeratotic poikiloderma of Kindler-Weary | (Orphanet:306539) |
Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
Lipodystrophy due to peptidic growth factors deficiency | (Orphanet:1979) |
METAPHYSEAL DYSPLASIA, ANETODERMA, AND OPTIC ATROPHY | (OMIM:250450) |
Mandibular hypoplasia-deafness-progeroid syndrome | (Orphanet:363649) |
Mandibuloacral dysplasia | (Orphanet:2457) |
Mandibuloacral dysplasia with type A lipodystrophy | (Orphanet:90153) |
Mandibuloacral dysplasia with type B lipodystrophy | (Orphanet:90154) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
Werner syndrome | (Orphanet:902) |
Wilson disease | (Orphanet:905) |
Xeroderma pigmentosum complementation group A | (Orphanet:276249) |
Xeroderma pigmentosum complementation group B | (Orphanet:276252) |
Xeroderma pigmentosum complementation group C | (Orphanet:276255) |
Xeroderma pigmentosum complementation group D | (Orphanet:276258) |
Xeroderma pigmentosum complementation group E | (Orphanet:276261) |
Xeroderma pigmentosum variant | (Orphanet:90342) |
Xeroderma pigmentosum/Cockayne syndrome complex | (Orphanet:220295) |