Advanced ossification of carpal bones

Symptom Information:

Symptom ID: HPO:0004233
Synonyms:
Accelerated carpal bone maturation [HPO:0004233]
Advanced carpal bone age [HPO:0004233]
Advanced carpal ossification [HPO:0004233]
Precociously ossified carpal bones [HPO:0004233]
Advanced bone age [Orphanet:45390]
Advanced bone age (finding) [Orphanet:45390]
Accelerated carpal bone maturation [OMIM:Accelerated carpal bone maturation]
Advanced carpal bone age [OMIM:Advanced carpal bone age]
Advanced carpal ossification [OMIM:Advanced carpal ossification]
Precociously ossified carpal bones [OMIM:Precociously ossified carpal bones]
Advanced bone age (in some patients) [OMIM:Advanced bone age (in some patients)]
Quality:
Cross references:
HPO:0005616 "Accelerated skeletal maturation" [Orphanet:45390]
Orphanet:45390 "Advanced bone age" [Orphanet:45390]
OMIM: "Accelerated carpal bone maturation" [OMIM:Accelerated carpal bone maturation]
OMIM: "Advanced carpal bone age" [OMIM:Advanced carpal bone age]
OMIM: "Advanced carpal ossification" [OMIM:Advanced carpal ossification]
OMIM: "Precociously ossified carpal bones" [OMIM:Precociously ossified carpal bones]
OMIM: "Advanced bone age (in some patients)" [OMIM:Advanced bone age (in some patients)]
UMLS:C0545053 "Advanced bone age" [Orphanet:45390]
Is a (Direct Parents):
HPO         Abnormality of carpal bone ossification
Orphanet Abnormality of the skeletal system
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal bone structure(HPO:0003330)
                Abnormal bone ossification(HPO:0011849)
                   Abnormal hand bone ossification(HPO:0010660)
                      Abnormality of carpal bone ossification(HPO:0006257)
                         Advanced ossification of carpal bones(HPO:0004233)
             Abnormal joint morphology(HPO:0001367)
                Abnormality of upper limb joint(HPO:0009810)
                   Abnormality of the wrist(HPO:0003019)
                      Abnormality of the carpal bones(HPO:0001191)
                         Abnormality of carpal bone ossification(HPO:0006257)
                            Advanced ossification of carpal bones(HPO:0004233)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the upper limb(HPO:0002817)
                      Abnormality of the hand(HPO:0001155)
                         Abnormality of the carpal bones(HPO:0001191)
                            Abnormality of carpal bone ossification(HPO:0006257)
                               Advanced ossification of carpal bones(HPO:0004233)
                         Abnormal hand bone ossification(HPO:0010660)
                            Abnormality of carpal bone ossification(HPO:0006257)
                               Advanced ossification of carpal bones(HPO:0004233)
                      Abnormality of upper limb joint(HPO:0009810)
                         Abnormality of the wrist(HPO:0003019)
                            Abnormality of the carpal bones(HPO:0001191)
                               Abnormality of carpal bone ossification(HPO:0006257)
                                  Advanced ossification of carpal bones(HPO:0004233)
MedDRA:
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

Alström syndrome (Orphanet:64)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
CORTISONE REDUCTASE DEFICIENCY 2 (OMIM:614662)
Chondrodysplasia, Blomstrand type (Orphanet:50945)
DESBUQUOIS DYSPLASIA 1 (OMIM:251450)
DESBUQUOIS DYSPLASIA 2 (OMIM:615777)
Desbuquois syndrome (Orphanet:1425)
Dyssegmental dysplasia, Rolland-Desbuquois type (Orphanet:156731)
EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 2 (OMIM:615349)
Insulin-resistance syndrome type A (Orphanet:2297)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1 (OMIM:608594)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 (OMIM:269700)
Schneckenbecken dysplasia (Orphanet:3144)
Spondyloepimetaphyseal dysplasia with joint laxity (Orphanet:93359)