Accelerated skeletal maturation
Symptom Information:
Symptom ID: | HPO:0005616 | ||||||||
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 skeletal system(HPO:0000924) Abnormality of skeletal physiology(HPO:0011843) Abnormality of skeletal maturation(HPO:0000927) Accelerated skeletal maturation(HPO:0005616) MedDRA: |
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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) |