Progeroid facial appearance

Symptom Information:

Symptom ID: HPO:0005328
Synonyms:
Aged facial appearance [HPO:0005328]
Prematurely aged face [HPO:0005328]
Prematurely aged facial appearance [HPO:0005328]
Wizened face [HPO:0005328]
Aged facial appearance [OMIM:Aged facial appearance]
Prematurely aged face [OMIM:Prematurely aged face]
Prematurely aged facial appearance [OMIM:Prematurely aged facial appearance]
Wizened face [OMIM:Wizened face]
Progeroid facial appearance (onset childhood) [OMIM:Progeroid facial appearance (onset childhood)]
Quality:
Cross references:
OMIM: "Aged facial appearance" [OMIM:Aged facial appearance]
OMIM: "Prematurely aged face" [OMIM:Prematurely aged face]
OMIM: "Prematurely aged facial appearance" [OMIM:Prematurely aged facial appearance]
OMIM: "Wizened face" [OMIM:Wizened face]
OMIM: "Progeroid facial appearance (onset childhood)" [OMIM:Progeroid facial appearance (onset childhood)]
Is a (Direct Parents):
HPO         Prematurely aged appearance
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)
                   Progeroid facial appearance(HPO:0005328)
MedDRA:
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive Emery-Dreifuss muscular dystrophy (Orphanet:98855)
COCKAYNE SYNDROME A (OMIM:216400)
COCKAYNE SYNDROME B (OMIM:133540)
Cockayne syndrome (Orphanet:191)
DERMATOLEUKODYSTROPHY (OMIM:221790)
GRANDDAD SYNDROME (OMIM:138920)
KEPPEN-LUBINSKY SYNDROME (OMIM:614098)
Leprechaunism (Orphanet:508)
Lipodystrophy - intellectual deficit - deafness (Orphanet:50811)
PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES (OMIM:602249)
Rabson-Mendenhall syndrome (Orphanet:769)
Werner syndrome (Orphanet:902)
Xeroderma pigmentosum complementation group B (Orphanet:276252)