Advanced ossification of carpal bones
Symptom Information:
Symptom ID: | HPO:0004233 | |||||||||||
Synonyms: |
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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 morphology(HPO:0011842) 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) 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) MedDRA: |
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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) |