Carpal synostosis

Symptom Information:

Symptom ID: HPO:0009702
Synonyms:
Carpal bone fusion [HPO:0009702]
Carpal fusion [HPO:0009702]
Fused carpal bones [HPO:0009702]
Synostosis involving the carpal bones [HPO:0009702]
Carpal bones synostosis [Orphanet:19780]
Carpal synostosis (disorder) [Orphanet:19780]
Carpal synostosis [Orphanet:19780]
Carpal bone fusion [OMIM:Carpal bone fusion]
Carpal fusion [OMIM:Carpal fusion]
Carpal synostosis [OMIM:Carpal synostosis]
Fused carpal bones [OMIM:Fused carpal bones]
Carpal bones fusion/synostosis [Orphanet:19780]
Carpal fusion (rare) [OMIM:Carpal fusion (rare)]
Carpal fusions [OMIM:Carpal fusions]
Carpal synostosis (especially capitate-hamate and lunate-triquetrum) [OMIM:Carpal synostosis (especially capitate-hamate and lunate-triquetrum)]
Quality:
Cross references:
HPO:0005048 "Synostosis of carpal bones" [Orphanet:19780]
Orphanet:19780 "Carpal bones fusion/synostosis" [Orphanet:19780]
OMIM: "Carpal bone fusion" [OMIM:Carpal bone fusion]
OMIM: "Carpal fusion" [OMIM:Carpal fusion]
OMIM: "Carpal synostosis" [OMIM:Carpal synostosis]
OMIM: "Fused carpal bones" [OMIM:Fused carpal bones]
OMIM: "Carpal fusion (rare)" [OMIM:Carpal fusion (rare)]
OMIM: "Carpal fusions" [OMIM:Carpal fusions]
OMIM: "Carpal synostosis (especially capitate-hamate and lunate-triquetrum)" [OMIM:Carpal synostosis (especially capitate-hamate and lunate-triquetrum)]
UMLS:C0431863 "Carpal synostosis" [Orphanet:19780]
Is a (Direct Parents):
HPO         Abnormality of the carpal bones
HPO         Synostosis involving bones of the hand
Orphanet Abnormality of the carpal bones
HPO         Synostosis of carpals/tarsals
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 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 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)
             Abnormal joint morphology(HPO:0001367)
                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)
                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)
MedDRA:
Database Frequency: 26 / 7739
Resource:

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)