Thin skin

Symptom Information:

Symptom ID: HPO:0000963
Synonyms:
Thin skin (finding) [Orphanet:23390]
Thin skin [Orphanet:23390]
Thin skin [OMIM:Thin skin]
Skin thinning of [Orphanet:23390]
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 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)]
Quality:
Cross references:
Orphanet:23390 "Thin skin" [Orphanet:23390]
OMIM: "Thin skin" [OMIM:Thin skin]
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)]
UMLS:C0423757 "Thin skin" [Orphanet:23390]
Is a (Direct Parents):
MedDRA Skin hypoplasias and atrophies
HPO         Aplasia/Hypoplasia of the skin
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)
             Localized skin lesion(HPO:0011355)
                Aplasia/Hypoplasia of the skin(HPO:0008065)
                   Thin skin(HPO:0000963)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Cornification and dystrophic skin disorders(MedDRA:10011063)
       Skin hypoplasias and atrophies(MedDRA:10040870)
          Thin skin(HPO:0000963)
Database Frequency: 96 / 7739
Resource:

All diseases associated with this symptom:

19q13.11 microdeletion syndrome (Orphanet:217346)
2q32q33 microdeletion syndrome (Orphanet:251019)
ACTH-dependent Cushing syndrome (Orphanet:99892)
ACTH-independent Cushing syndrome (Orphanet:99893)
ACTH-independent macronodular adrenal hyperplasia (Orphanet:189427)
ADULT syndrome (Orphanet:978)
Ablepharon macrostomia syndrome (Orphanet:920)
Absence of fingerprints - congenital milia (Orphanet:1658)
Acrofacial dysostosis, Rodriguez type (Orphanet:1788)
Acrogeria (Orphanet:2500)
Albright hereditary osteodystrophy (Orphanet:665)
Arterial tortuosity syndrome (Orphanet:3342)
Autosomal dominant hypohidrotic ectodermal dysplasia (Orphanet:1810)
Blepharophimosis-intellectual deficit syndrome due to UBE3B deficiency (Orphanet:329255)
CHILD syndrome (Orphanet:139)
COCOON SYNDROME (OMIM:613630)
Carney complex (Orphanet:1359)
Coats plus syndrome (Orphanet:313838)
Congenital osteogenesis imperfecta - microcephaly - cataracts (Orphanet:2772)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
Cushing syndrome due to ectopic ACTH secretion (Orphanet:99889)
DK1-CDG (Orphanet:91131)
De Barsy syndrome (Orphanet:2962)
Dermo-odonto dysplasia (Orphanet:1660)
Diaphyseal medullary stenosis - bone malignancy (Orphanet:85182)
Dystrophic epidermolysis bullosa pruriginosa (Orphanet:89843)
EEC syndrome (Orphanet:1896)
Ear-patella-short stature syndrome (Orphanet:2554)
Ectodermal dysplasia - intellectual deficit - central nervous system malformation (Orphanet:1812)
Ehlers-Danlos syndrome due to tenascin-X deficiency (Orphanet:230839)
Ehlers-Danlos syndrome type 1 (Orphanet:90309)
Ehlers-Danlos syndrome type 2 (Orphanet:90318)
Ehlers-Danlos syndrome type 7A (Orphanet:99875)
Ehlers-Danlos syndrome with periventricular heterotopia (Orphanet:82004)
Ehlers-Danlos syndrome, arthrochalasic type (Orphanet:1899)
Ehlers-Danlos syndrome, cardiac valvular type (Orphanet:230851)
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, spondylocheirodysplastic type (Orphanet:157965)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Familial partial lipodystrophy, Dunnigan type (Orphanet:2348)
Focal dermal hypoplasia (Orphanet:2092)
Geroderma osteodysplastica (Orphanet:2078)
Hallermann-Streiff syndrome (Orphanet:2108)
Hepatoerythropoietic porphyria (Orphanet:95159)
Hereditary acrokeratotic poikiloderma, Weary type (Orphanet:2907)
Hereditary coproporphyria (Orphanet:79273)
Hereditary thrombophilia due to congenital protein C deficiency (Orphanet:745)
Hereditary thrombophilia due to congenital protein S deficiency (Orphanet:743)
Hutchinson-Gilford progeria syndrome (Orphanet:740)
Hydrocephalus - blue sclerae - nephropathy (Orphanet:2186)
Hypohidrotic ectodermal dysplasia (Orphanet:238468)
Hypotrichosis - lymphedema - telangiectasia (Orphanet:69735)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Lipodystrophy due to peptidic growth factors deficiency (Orphanet:1979)
Loeys-Dietz syndrome type 1 (Orphanet:60030)
MEIER-GORLIN SYNDROME 1 (OMIM:224690)
MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,AND PSYCHOMOTOR DELAY (OMIM:601347)
Mandibuloacral dysplasia (Orphanet:2457)
Mandibuloacral dysplasia with type A lipodystrophy (Orphanet:90153)
Mandibuloacral dysplasia with type B lipodystrophy (Orphanet:90154)
Marshall-Smith syndrome (Orphanet:561)
Mucolipidosis type 2 (Orphanet:576)
OSTEOGENESIS IMPERFECTA, TYPE I (OMIM:166200)
OSTEOGENESIS IMPERFECTA, TYPE II (OMIM:166210)
Oculocerebral hypopigmentation syndrome, Cross type (Orphanet:2719)
Osteogenesis imperfecta type 1 (Orphanet:216796)
Osteogenesis imperfecta type 2 (Orphanet:216804)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1 (OMIM:610489)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2 (OMIM:610475)
PYCR1-related DeBarsy syndrome (Orphanet:293633)
Porphyria cutanea tarda (Orphanet:101330)
Porphyria due to ALA dehydratase deficiency (Orphanet:100924)
Porphyria variegata (Orphanet:79473)
Primary lipodystrophy (Orphanet:90970)
Primary pigmented nodular adrenocortical disease (Orphanet:189439)
Prolidase deficiency (Orphanet:742)
Pseudoprogeria syndrome (Orphanet:2985)
RAPP-HODGKIN SYNDROME (OMIM:129400)
Retinal ischemic syndrome - digestive tract small vessel hyalinosis - diffuse cerebral calcifications (Orphanet:3018)
SHORT syndrome (Orphanet:3163)
Stoll-Alembik-Finck syndrome (Orphanet:3200)
Stüve-Wiedemann syndrome (Orphanet:3206)
Superficial epidermolytic ichthyosis (Orphanet:455)
Transaldolase deficiency (Orphanet:101028)
Transient bullous dermolysis of the newborn (Orphanet:79411)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)
X-linked Ehlers-Danlos syndrome (Orphanet:75497)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)
Xeroderma pigmentosum (Orphanet:910)