Prematurely aged appearance

Symptom Information:

Symptom ID: HPO:0007495
Synonyms:
Precociously senile appearance [HPO:0007495]
Premature ageing [Orphanet:53700]
Premature aging syndrome (disorder) [Orphanet:53700]
Premature aging (finding) [Orphanet:53700]
Premature aging syndrome [Orphanet:53700]
Precociously senile appearance [OMIM:Precociously senile appearance]
Prematurely aged appearance [OMIM:Prematurely aged appearance]
Premature ageing [MedDRA:10063493]
Premature aging [MedDRA:10063493]
Quality:
Cross references:
Orphanet:53700 "Premature ageing" [Orphanet:53700]
OMIM: "Precociously senile appearance" [OMIM:Precociously senile appearance]
OMIM: "Prematurely aged appearance" [OMIM:Prematurely aged appearance]
UMLS:C0231341 "Premature aging syndrome" [Orphanet:53700]
Is a (Direct Parents):
HPO         Generalized abnormality of skin
Orphanet Build/stature/longevity anomalies
MedDRA General signs and symptoms NEC
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)
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)