Joint contracture of the hand

Symptom Information:

Symptom ID: HPO:0009473
Synonyms:
Contractures involving the hands [HPO:0009473]
Contractures of the hands [HPO:0009473]
Contracture of joint of hand [HPO:0009473]
Contractures of the hands [OMIM:Contractures of the hands]
Contracture of hand joint [HPO:0009473]
Joint contracture [MedDRA:10023201]
Contracture of ankle and foot joint [MedDRA:10023201]
Contracture of forearm joint [MedDRA:10023201]
Contracture of hand joint [MedDRA:10023201]
Contracture of joint [MedDRA:10023201]
Contracture of joint of multiple sites [MedDRA:10023201]
Contracture of joint of other specified sites [MedDRA:10023201]
Contracture of joint of pelvic region and thigh [MedDRA:10023201]
Contracture of joint of shoulder region [MedDRA:10023201]
Contracture of joint, site unspecified [MedDRA:10023201]
Contracture of lower leg joint [MedDRA:10023201]
Contracture of upper arm joint [MedDRA:10023201]
Joint contractures (elbows and knees) [OMIM:Joint contractures (elbows and knees)]
Joint contractures (elbows, fingers, knees) [OMIM:Joint contractures (elbows, fingers, knees)]
Joint contractures (fingers, hips, knees) [OMIM:Joint contractures (fingers, hips, knees)]
Joint contractures (improves with time) [OMIM:Joint contractures (improves with time)]
Joint contractures (in 1 patient) [OMIM:Joint contractures (in 1 patient)]
Joint contractures (in some patients) [OMIM:Joint contractures (in some patients)]
Joint contractures (less common) [OMIM:Joint contractures (less common)]
Joint contractures (small and large joints affected) [OMIM:Joint contractures (small and large joints affected)]
Joint contractures (with age) [OMIM:Joint contractures (with age)]
Quality:
Cross references:
OMIM: "Contractures of the hands" [OMIM:Contractures of the hands]
OMIM: "Joint contractures (elbows and knees)" [OMIM:Joint contractures (elbows and knees)]
OMIM: "Joint contractures (elbows, fingers, knees)" [OMIM:Joint contractures (elbows, fingers, knees)]
OMIM: "Joint contractures (fingers, hips, knees)" [OMIM:Joint contractures (fingers, hips, knees)]
OMIM: "Joint contractures (improves with time)" [OMIM:Joint contractures (improves with time)]
OMIM: "Joint contractures (in 1 patient)" [OMIM:Joint contractures (in 1 patient)]
OMIM: "Joint contractures (in some patients)" [OMIM:Joint contractures (in some patients)]
OMIM: "Joint contractures (less common)" [OMIM:Joint contractures (less common)]
OMIM: "Joint contractures (small and large joints affected)" [OMIM:Joint contractures (small and large joints affected)]
OMIM: "Joint contractures (with age)" [OMIM:Joint contractures (with age)]
Is a (Direct Parents):
HPO         Contractures of the joints of the upper limbs
MedDRA Joint related disorders NEC
HPO         Abnormality of upper limb joint
HPO         Flexion contracture of finger
HPO         Abnormality of the hand
HPO         Bethlem sign
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle morphology(HPO:0011805)
             Flexion contracture(HPO:0001371)
                Limb joint contracture(HPO:0003121)
                   Contractures of the joints of the upper limbs(HPO:0100360)
                      Joint contracture of the hand(HPO:0009473)
       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)
                   Joint contracture of the hand(HPO:0009473)
                Abnormality of joint mobility(HPO:0011729)
                   Flexion contracture(HPO:0001371)
                      Limb joint contracture(HPO:0003121)
                         Contractures of the joints of the upper limbs(HPO:0100360)
                            Joint contracture of the hand(HPO:0009473)
             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)
                         Joint contracture of the hand(HPO:0009473)
                      Abnormality of upper limb joint(HPO:0009810)
                         Joint contracture of the hand(HPO:0009473)
       Abnormality of connective tissue(HPO:0003549)
          Flexion contracture(HPO:0001371)
             Limb joint contracture(HPO:0003121)
                Contractures of the joints of the upper limbs(HPO:0100360)
                   Joint contracture of the hand(HPO:0009473)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Joint disorders(MedDRA:10023213)
       Joint related disorders NEC(MedDRA:10027685)
          Joint contracture of the hand(HPO:0009473)
Database Frequency: 84 / 7739
Resource:

All diseases associated with this symptom:

2p15p16.1 microdeletion syndrome (Orphanet:261349)
8q22.1 microdeletion syndrome (Orphanet:178303)
ALG13-CDG (Orphanet:324422)
ALG3-CDG (Orphanet:79321)
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS (OMIM:201750)
ARTHROGRYPOSIS, DISTAL, TYPE 1B (OMIM:614335)
ARTHROGRYPOSIS, DISTAL, TYPE 2E (OMIM:121070)
ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLYDEATH (OMIM:208910)
ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 3 (OMIM:170995)
Allan-Herndon-Dudley syndrome (Orphanet:59)
Alopecia - contractures - dwarfism - intellectual deficit (Orphanet:1005)
Autosomal recessive lower motor neuron disease with childhood onset (Orphanet:206580)
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA (OMIM:609945)
Bathing suit ichthyosis (Orphanet:100976)
Brachydactyly type B (Orphanet:93383)
CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III (OMIM:611929)
CAMPTODACTYLY WITH FIBROUS TISSUE HYPERPLASIA AND SKELETAL DYSPLASIA (OMIM:211930)
COFS syndrome (Orphanet:1466)
CORPUS CALLOSUM, AGENESIS OF (OMIM:217990)
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG (OMIM:218649)
Camptodactyly - tall stature - scoliosis - hearing loss (Orphanet:85164)
Carpenter syndrome (Orphanet:65759)
Catel-Manzke syndrome (Orphanet:1388)
Congenital erythropoietic porphyria (Orphanet:79277)
Congenital lethal myopathy, Compton-North type (Orphanet:210163)
Dermato-cardio-skeletal syndrome, Borrone type (Orphanet:1266)
Dermatoosteolysis, Kirghizian type (Orphanet:1657)
Desmosterolosis (Orphanet:35107)
Digitotalar dysmorphism (Orphanet:1146)
Dyssegmental dysplasia, Rolland-Desbuquois type (Orphanet:156731)
EEM syndrome (Orphanet:1897)
Ear-patella-short stature syndrome (Orphanet:2554)
Ectodermal dysplasia - sensorineural deafness (Orphanet:1883)
Familial Dupuytren contracture (Orphanet:79142)
Fibrochondrogenesis (Orphanet:2021)
Freeman-Sheldon syndrome (Orphanet:2053)
Frontonasal dysplasia (Orphanet:250)
Fryns syndrome (Orphanet:2059)
Galloway-Mowat syndrome (Orphanet:2065)
Goodman syndrome (Orphanet:65798)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
HUNTER-MACDONALD SYNDROME (OMIM:611962)
Hennekam syndrome (Orphanet:2136)
Intellectual deficit - cataracts - calcified pinnae - myopathy (Orphanet:3042)
KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS (OMIM:245160)
Kapur-Toriello syndrome (Orphanet:2328)
LOEYS-DIETZ SYNDROME 2 (OMIM:610168)
Leukoencephalopathy with brain stem and spinal cord involvement - lactate elevation (Orphanet:137898)
Limb-mammary syndrome (Orphanet:69085)
Loeys-Dietz syndrome type 1 (Orphanet:60030)
MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT (OMIM:608257)
MICROPHTHALMIA, SYNDROMIC 1 (OMIM:309800)
MIDLINE MALFORMATIONS, MULTIPLE, WITH LIMB ABNORMALITIES AND HYPOPITUITARISM (OMIM:601016)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 6 (OMIM:608840)
MYOPATHY, DISTAL, 3 (OMIM:610099)
Marden-Walker syndrome (Orphanet:2461)
Metatropic dysplasia (Orphanet:2635)
Miller-Dieker syndrome (Orphanet:531)
Neu-Laxova syndrome (Orphanet:2671)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE (OMIM:258650)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER) (OMIM:214110)
Pelviscapular dysplasia (Orphanet:93333)
Pontocerebellar hypoplasia type 8 (Orphanet:324569)
Posterior column ataxia - retinitis pigmentosa (Orphanet:88628)
Pseudoaminopterin syndrome (Orphanet:221120)
Recombinant 8 syndrome (Orphanet:96167)
Renpenning syndrome (Orphanet:3242)
STEVENSON-CAREY SYNDROME (OMIM:611961)
Scheie syndrome (Orphanet:93474)
Schwartz-Jampel syndrome (Orphanet:800)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Syndactyly type 5 (Orphanet:93406)
Tel Hashomer camptodactyly syndrome (Orphanet:3292)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)
URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME (OMIM:300280)
Urban-Rogers-Meyer syndrome (Orphanet:3409)
Van den Ende-Gupta syndrome (Orphanet:2460)
W syndrome (Orphanet:2804)
Weaver syndrome (Orphanet:3447)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)
Xeroderma pigmentosum complementation group F (Orphanet:276264)
Zunich-Kaye syndrome (Orphanet:3474)