Accelerated skeletal maturation

Symptom Information:

Symptom ID: HPO:0005616
Synonyms:
Advanced bone age [HPO:0005616]
Early bone maturation [HPO:0005616]
Advanced bone age [Orphanet:45390]
Advanced bone age (finding) [Orphanet:45390]
Advanced bone age [OMIM:Advanced bone age]
Accelerated skeletal maturation (bone age of 4 at birth) [OMIM:Accelerated skeletal maturation (bone age of 4 at birth)]
Advanced bone age (in some patients) [OMIM:Advanced bone age (in some patients)]
Early bone maturation (in some patients) [OMIM:Early bone maturation (in some patients)]
Quality:
Cross references:
HPO:0004233 "Advanced ossification of carpal bones" [Orphanet:45390]
Orphanet:45390 "Advanced bone age" [Orphanet:45390]
OMIM: "Advanced bone age" [OMIM:Advanced bone age]
OMIM: "Accelerated skeletal maturation (bone age of 4 at birth)" [OMIM:Accelerated skeletal maturation (bone age of 4 at birth)]
OMIM: "Advanced bone age (in some patients)" [OMIM:Advanced bone age (in some patients)]
OMIM: "Early bone maturation (in some patients)" [OMIM:Early bone maturation (in some patients)]
UMLS:C0545053 "Advanced bone age" [Orphanet:45390]
Is a (Direct Parents):
HPO         Abnormality of skeletal maturation
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 physiology(HPO:0011843)
             Abnormality of skeletal maturation(HPO:0000927)
                Accelerated skeletal maturation(HPO:0005616)
MedDRA:
Database Frequency: 46 / 7739
Resource:

All diseases associated with this symptom:

ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE (OMIM:101800)
ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE (OMIM:614613)
Acrodysostosis (Orphanet:950)
Acrodysostosis with multiple hormone resistance (Orphanet:280651)
Alström syndrome (Orphanet:64)
Aromatase excess syndrome (Orphanet:178345)
Beckwith-Wiedemann syndrome (Orphanet:116)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
CHROMOSOME Xq26.3 DUPLICATION SYNDROME (OMIM:300942)
CORTISONE REDUCTASE DEFICIENCY 2 (OMIM:614662)
Cartilage-hair hypoplasia (Orphanet:175)
Cerebral gigantism - jaw cysts (Orphanet:2081)
Chondrodysplasia, Blomstrand type (Orphanet:50945)
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (Orphanet:90794)
Congenital adrenal hyperplasia (Orphanet:418)
Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency (Orphanet:90795)
Desbuquois syndrome (Orphanet:1425)
Dysplasia epiphysealis hemimelica (Orphanet:1822)
EDINBURGH MALFORMATION SYNDROME (OMIM:129850)
Edinburgh malformation syndrome (Orphanet:1895)
Familial glucocorticoid deficiency (Orphanet:361)
Familial hyperthyroidism due to mutations in TSH receptor (Orphanet:424)
Frontometaphyseal dysplasia (Orphanet:1826)
GLUCOCORTICOID DEFICIENCY 1 (OMIM:202200)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
Heart defects - limb shortening (Orphanet:1354)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
Insulin-resistance syndrome type A (Orphanet:2297)
Intellectual deficit - sparse hair - brachydactyly (Orphanet:3051)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1 (OMIM:608594)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 (OMIM:269700)
Larsen-like syndrome, B3GAT3 type (Orphanet:284139)
Marshall-Smith syndrome (Orphanet:561)
Metaphyseal acroscyphodysplasia (Orphanet:1240)
Monosomy 22q13 (Orphanet:48652)
Monosomy 9q22.3 (Orphanet:77301)
PRECOCIOUS PUBERTY, CENTRAL, 2 (OMIM:615346)
SOTOS SYNDROME 1 (OMIM:117550)
SOTOS SYNDROME 2 (OMIM:614753)
Schneckenbecken dysplasia (Orphanet:3144)
Short rib-polydactyly syndrome (Orphanet:1505)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Sotos syndrome (Orphanet:821)
Spondylometaphyseal dysplasia, Sedaghatian type (Orphanet:93317)
Testotoxicosis (Orphanet:3000)
Weaver syndrome (Orphanet:3447)