Carpal synostosis
Symptom Information:
Symptom ID: | HPO:0009702 | |||||||||||||||
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 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) Synostosis involving bones of the hand(HPO:0004278) Carpal synostosis(HPO:0009702) Abnormality of the carpal bones(HPO:0001191) Carpal synostosis(HPO:0009702) Abnormality of upper limb joint(HPO:0009810) Abnormality of the wrist(HPO:0003019) Abnormality of the carpal bones(HPO:0001191) Carpal synostosis(HPO:0009702) Synostosis involving bones of the upper limbs(HPO:0100238) Synostosis involving bones of the hand(HPO:0004278) Carpal synostosis(HPO:0009702) 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) Carpal synostosis(HPO:0009702) Synostosis involving bones of the upper limbs(HPO:0100238) Synostosis involving bones of the hand(HPO:0004278) Carpal synostosis(HPO:0009702) Abnormality of joint mobility(HPO:0011729) Synostosis of joints(HPO:0100240) Synostosis involving bones of the upper limbs(HPO:0100238) Synostosis involving bones of the hand(HPO:0004278) Carpal synostosis(HPO:0009702) Synostosis of carpals/tarsals(HPO:0100266) Carpal synostosis(HPO:0009702) MedDRA: |
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Database Frequency: | 26 / 7739 | |||||||||||||||
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All diseases associated with this symptom:
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS | (OMIM:201750) |
Baller-Gerold syndrome | (Orphanet:1225) |
Brachydactyly type A6 | (Orphanet:93382) |
Brachydactyly type B2 | (Orphanet:140908) |
CHONDRODYSPLASIA, ACROMESOMELIC, WITH GENITAL ANOMALIES | (OMIM:609441) |
EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 2 | (OMIM:615349) |
HUMERORADIAL SYNOSTOSIS WITH CRANIOFACIAL ANOMALIES | (OMIM:236410) |
IVIC syndrome | (Orphanet:2307) |
MULTIPLE SYNOSTOSES SYNDROME 1 | (OMIM:186500) |
MULTIPLE SYNOSTOSES SYNDROME 2 | (OMIM:610017) |
Mesomelic dysplasia, Kantaputra type | (Orphanet:1836) |
Multiple synostoses syndrome | (Orphanet:3237) |
OTOFACIOOSSEOUS-GONADAL SYNDROME | (OMIM:601976) |
Proximal symphalangism | (Orphanet:3250) |
SYMPHALANGISM, PROXIMAL, 1A | (OMIM:185800) |
SYNOSTOSES, TARSAL, CARPAL, AND DIGITAL | (OMIM:186400) |
Spondylocarpotarsal synostosis | (Orphanet:3275) |
Spondyloepimetaphyseal dysplasia with joint laxity | (Orphanet:93359) |
Syndactyly type 5 | (Orphanet:93406) |
Synpolydactyly type 2 | (Orphanet:295197) |
TARSAL-CARPAL COALITION SYNDROME | (OMIM:186570) |
TUKEL SYNDROME | (OMIM:609428) |
Tarsal-carpal coalition syndrome | (Orphanet:1412) |
Temtamy preaxial brachydactyly syndrome | (Orphanet:363417) |
Thrombocytopenia - absent radius | (Orphanet:3320) |
Waardenburg syndrome | (Orphanet:3440) |