Prematurely aged appearance
Symptom Information:
Symptom ID: | HPO:0007495 | |||||||||
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) Generalized abnormality of skin(HPO:0011354) Prematurely aged appearance(HPO:0007495) MedDRA: General disorders and administration site conditions(MedDRA:10018065) General system disorders NEC(MedDRA:10018073) General signs and symptoms NEC(MedDRA:10018072) Prematurely aged appearance(HPO:0007495) |
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Database Frequency: | 44 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
Acrogeria | (Orphanet:2500) |
Arterial tortuosity syndrome | (Orphanet:3342) |
Ataxia-telangiectasia | (Orphanet:100) |
Autosomal dominant cutis laxa | (Orphanet:90348) |
Autosomal recessive cutis laxa type 1 | (Orphanet:90349) |
Bird headed-dwarfism, Montreal type | (Orphanet:2617) |
COCKAYNE SYNDROME A | (OMIM:216400) |
COCKAYNE SYNDROME B | (OMIM:133540) |
COCKAYNE SYNDROME, TYPE III | (OMIM:216411) |
Campomelia, Cumming type | (Orphanet:1318) |
Cataract - intellectual deficit - hypogonadism | (Orphanet:1387) |
Cockayne syndrome | (Orphanet:191) |
Cutis laxa | (Orphanet:209) |
De Barsy syndrome | (Orphanet:2962) |
Down syndrome | (Orphanet:870) |
Ehlers-Danlos syndrome, progeroid type | (Orphanet:75496) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
Epidermolysis bullosa simplex with mottled pigmentation | (Orphanet:79397) |
Facial ectodermal dysplasia | (Orphanet:1807) |
GAPO syndrome | (Orphanet:2067) |
Geroderma osteodysplastica | (Orphanet:2078) |
Hutchinson-Gilford progeria syndrome | (Orphanet:740) |
LMNA-related cardiocutaneous progeria syndrome | (Orphanet:363618) |
Laron syndrome | (Orphanet:633) |
Lenz-Majewski hyperostotic dwarfism | (Orphanet:2658) |
MACROEPIPHYSEAL DYSPLASIA WITH OSTEOPOROSIS, WRINKLED SKIN, AND AGEDAPPEARANCE | (OMIM:248010) |
Mandibuloacral dysplasia | (Orphanet:2457) |
Mandibuloacral dysplasia with type A lipodystrophy | (Orphanet:90153) |
Mandibuloacral dysplasia with type B lipodystrophy | (Orphanet:90154) |
Partial acquired lipodystrophy | (Orphanet:79087) |
Progeria - short stature - pigmented nevi | (Orphanet:2959) |
Progeroid syndrome, Petty type | (Orphanet:2963) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Rothmund-Thomson syndrome type 1 | (Orphanet:221008) |
Rothmund-Thomson syndrome type 2 | (Orphanet:221016) |
STORM SYNDROME | (OMIM:185069) |
Seckel syndrome | (Orphanet:808) |
Short stature - intellectual deficit - eye anomalies - cleft lip/palate | (Orphanet:2649) |
Werner syndrome | (Orphanet:902) |
Wiedemann-Rautenstrauch syndrome | (Orphanet:3455) |
Williams syndrome | (Orphanet:904) |
Wrinkly skin syndrome | (Orphanet:2834) |
XFE PROGEROID SYNDROME | (OMIM:610965) |
Xeroderma pigmentosum/Cockayne syndrome complex | (Orphanet:220295) |