Dermal atrophy

Symptom Information:

Symptom ID: HPO:0004334
Synonyms:
Atrophic skin [HPO:0004334]
Skin atrophy [HPO:0004334]
Skin atrophy [Orphanet:23050]
Atrophic condition of skin [HPO:0004334]
Aplasia of skin (disorder) [Orphanet:23050]
Atrophic condition of skin (disorder) [Orphanet:23050]
Atrophoderma (disorder) [Orphanet:23430]
Atrophic condition of skin (disorder) [Orphanet:23430]
Skin hypoplasia [Orphanet:23050]
Atrophic condition of skin [Orphanet:23050]
Atrophic condition of skin [Orphanet:23430]
Atrophic skin [OMIM:Atrophic skin]
Skin atrophy [OMIM:Skin atrophy]
Skin hypoplasia/aplasia/atrophy [Orphanet:23050]
Anetodermia/dermal atrophy [Orphanet:23430]
Skin atrophy [Orphanet:23430]
Skin atrophy [MedDRA:10040799]
Atrophy skin [MedDRA:10040799]
Crepy skin [MedDRA:10040799]
Loss of skin elasticity [MedDRA:10040799]
Senile skin atrophy [MedDRA:10040799]
Skin atrophy senile [MedDRA:10040799]
Skin thinness [MedDRA:10040799]
Skin thinning of [MedDRA:10040799]
Skin hypoplasia [MedDRA:10040869]
Skin atrophy (especially over hands and feet) [OMIM:Skin atrophy (especially over hands and feet)]
Skin atrophy (over nose and scalp sutural areas) [OMIM:Skin atrophy (over nose and scalp sutural areas)]
Anetoderma [Orphanet:23430]
Anetoderma (disorder) [Orphanet:23430]
Atrophoderma maculatum (disorder) [Orphanet:23430]
Atrophoderma maculatum [Orphanet:23430]
Anetoderma (macular atrophy of skin) [OMIM:Anetoderma (macular atrophy of skin)]
Quality:
Cross references:
Orphanet:23050 "Skin hypoplasia/aplasia/atrophy" [Orphanet:23050]
Orphanet:23430 "Anetodermia/dermal atrophy" [Orphanet:23430]
OMIM: "Atrophic skin" [OMIM:Atrophic skin]
OMIM: "Skin atrophy" [OMIM:Skin atrophy]
OMIM: "Skin atrophy (especially over hands and feet)" [OMIM:Skin atrophy (especially over hands and feet)]
OMIM: "Skin atrophy (over nose and scalp sutural areas)" [OMIM:Skin atrophy (over nose and scalp sutural areas)]
OMIM: "Anetoderma (macular atrophy of skin)" [OMIM:Anetoderma (macular atrophy of skin)]
UMLS:C0235937 "Skin hypoplasia" [Orphanet:23050]
UMLS:C0151514 "Atrophic condition of skin" [Orphanet:23050]
UMLS:C0151514 "Atrophic condition of skin" [Orphanet:23430]
UMLS:C1288283 "Atrophoderma maculatum" [Orphanet:23430]
Is a (Direct Parents):
Orphanet Abnormality of the skin
HPO         Aplasia/Hypoplasia of the skin
MedDRA Skin hypoplasias and atrophies
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)
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)