Joint contracture of the hand
Symptom Information:
Symptom ID: | HPO:0009473 | ||||||||||||||||||||||||||
Synonyms: |
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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 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) Abnormality of the skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal joint morphology(HPO:0001367) 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) Abnormality of upper limb joint(HPO:0009810) 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 upper limb joint(HPO:0009810) Joint contracture of the hand(HPO:0009473) Abnormality of the hand(HPO:0001155) Joint contracture of the hand(HPO:0009473) 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) 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) |
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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) |