Thin skin
Symptom Information:
Symptom ID: | HPO:0000963 | ||||||||||||||
Synonyms: |
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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) 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) |
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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) |