Joint stiffness

Symptom Information:

Symptom ID: HPO:0001387
Synonyms:
Joint stiffness (hands, shoulder, elbows, knees, and ankles) [HPO:0001387]
Mild joint stiffness [HPO:0001387]
Stiff joint [HPO:0001387]
Stiff joints [HPO:0001387]
Joint stiffness (finding) [Orphanet:46200]
Joint stiffness [Orphanet:46200]
Joint stiffness [OMIM:Joint stiffness]
Joint stiffness (hands, shoulder, elbows, knees, and ankles) [OMIM:Joint stiffness (hands, shoulder, elbows, knees, and ankles)]
Mild joint stiffness [OMIM:Mild joint stiffness]
Stiff joints [OMIM:Stiff joints]
Restricted joint mobility/joint stiffness/ankylosis [Orphanet:46200]
Joint stiffness [MedDRA:10023230]
Ankle stiffness [MedDRA:10023230]
Early morning joint stiffness [MedDRA:10023230]
Jaw joint rigid state of [MedDRA:10023230]
Jaw stiffness [MedDRA:10023230]
Shoulder region stiffness of joint, not elsewhere classified, involving upper arm [MedDRA:10023230]
Stiff joint [MedDRA:10023230]
Stiff knees [MedDRA:10023230]
Stiffness joints [MedDRA:10023230]
Stiffness of joint, not elsewhere classified [MedDRA:10023230]
Stiffness of joint, not elsewhere classified, involving ankle and foot [MedDRA:10023230]
Stiffness of joint, not elsewhere classified, involving forearm [MedDRA:10023230]
Stiffness of joint, not elsewhere classified, involving hand [MedDRA:10023230]
Stiffness of joint, not elsewhere classified, involving lower leg [MedDRA:10023230]
Stiffness of joint, not elsewhere classified, involving multiple sites [MedDRA:10023230]
Stiffness of joint, not elsewhere classified, involving other specified sites [MedDRA:10023230]
Stiffness of joint, not elsewhere classified, involving pelvic region and thigh [MedDRA:10023230]
Stiffness of joint, not elsewhere classified, involving shoulder region [MedDRA:10023230]
Stiffness of joint, not elsewhere classified, involving unspecified site [MedDRA:10023230]
Stiffness of joint, not elsewhere classified, involving upper arm [MedDRA:10023230]
Stiffness hip [MedDRA:10023230]
Joint tightness [MedDRA:10023230]
Arthrosclerosis [MedDRA:10023230]
Joint stiffness (neck, shoulder, elbow, hips) [OMIM:Joint stiffness (neck, shoulder, elbow, hips)]
Joint ankylosis [MedDRA:10023198]
Ankylosis of joint (disorder) [Orphanet:46200]
Joint ankylosis [OMIM:Joint ankylosis]
Quality:
Cross references:
Orphanet:46200 "Restricted joint mobility/joint stiffness/ankylosis" [Orphanet:46200]
OMIM: "Joint stiffness" [OMIM:Joint stiffness]
OMIM: "Joint stiffness (hands, shoulder, elbows, knees, and ankles)" [OMIM:Joint stiffness (hands, shoulder, elbows, knees, and ankles)]
OMIM: "Mild joint stiffness" [OMIM:Mild joint stiffness]
OMIM: "Stiff joints" [OMIM:Stiff joints]
OMIM: "Joint stiffness (neck, shoulder, elbow, hips)" [OMIM:Joint stiffness (neck, shoulder, elbow, hips)]
OMIM: "Joint ankylosis" [OMIM:Joint ankylosis]
UMLS:C0162298 "Joint stiffness" [Orphanet:46200]
Is a (Direct Parents):
Orphanet Abnormal cartilage morphology
MedDRA Joint related signs and symptoms
HPO         Limitation of joint mobility
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 joint mobility(HPO:0011729)
                   Limitation of joint mobility(HPO:0001376)
                      Joint stiffness(HPO:0001387)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Joint disorders(MedDRA:10023213)
       Joint related signs and symptoms(MedDRA:10023226)
          Joint stiffness(HPO:0001387)
Database Frequency: 322 / 7739
Resource:

All diseases associated with this symptom:

17q23.1q23.2 microdeletion syndrome (Orphanet:261279)
3q13 microdeletion syndrome (Orphanet:1621)
8q22.1 microdeletion syndrome (Orphanet:178303)
Aase-Smith syndrome (Orphanet:916)
Achondroplasia (Orphanet:15)
Acromesomelic dysplasia, Grebe type (Orphanet:2098)
Acromesomelic dysplasia, Hunter-Thomson type (Orphanet:968)
Acromesomelic dysplasia, Maroteaux type (Orphanet:40)
Acromicric dysplasia (Orphanet:969)
Adult polyglucosan body disease (Orphanet:206583)
Alkaptonuria (Orphanet:56)
Allan-Herndon-Dudley syndrome (Orphanet:59)
Alopecia - contractures - dwarfism - intellectual deficit (Orphanet:1005)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Amish lethal microcephaly (Orphanet:99742)
Antecubital pterygium syndrome (Orphanet:2987)
Antley-Bixler syndrome (Orphanet:83)
Arthrogryposis - hyperkeratosis, lethal form (Orphanet:1485)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
Arthrogryposis due to muscular dystrophy (Orphanet:1155)
Arthrogryposis multiplex congenita - whistling face (Orphanet:1150)
Arthrogryposis with oculomotor limitation and electroretinal anomalies (Orphanet:1154)
Arthrogryposis-like hand anomaly - sensorineural deafness (Orphanet:1144)
Arthrogryposis-like syndrome (Orphanet:1149)
Aspartylglucosaminuria (Orphanet:93)
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy (Orphanet:1192)
Atypical teratoid tumor (Orphanet:99966)
Autosomal dominant congenital benign spinal muscular atrophy (Orphanet:1216)
Autosomal dominant popliteal pterygium syndrome (Orphanet:1300)
Autosomal dominant striatal neurodegeneration (Orphanet:228169)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
Autosomal recessive palmoplantar keratoderma and congenital alopecia (Orphanet:1366)
Babesiosis (Orphanet:108)
Baraitser-Winter syndrome (Orphanet:2995)
Bethlem myopathy (Orphanet:610)
Blau syndrome (Orphanet:90340)
Blepharophimosis - radioulnar synostosis (Orphanet:1256)
Bohring-Opitz syndrome (Orphanet:97297)
Bowen-Conradi syndrome (Orphanet:1270)
Brachydactyly - elbow wrist dysplasia (Orphanet:1275)
Brachydactyly-long thumb syndrome (Orphanet:2946)
Brachytelephalangy - dysmorphism - Kallmann syndrome (Orphanet:1295)
Bruck syndrome (Orphanet:2771)
Buschke-Ollendorff syndrome (Orphanet:1306)
C syndrome (Orphanet:1308)
CINCA syndrome (Orphanet:1451)
COFS syndrome (Orphanet:1466)
Camptodactyly - joint contractures - facial skeletal defects (Orphanet:1323)
Camurati-Engelmann disease (Orphanet:1328)
Cardiocranial syndrome, Pfeiffer type (Orphanet:2872)
Cardiomyopathy-cataract-hip spine disease (Orphanet:1345)
Cartilage-hair hypoplasia (Orphanet:175)
Catel-Manzke syndrome (Orphanet:1388)
Caudal regression sequence (Orphanet:3027)
Cerebrotendinous xanthomatosis (Orphanet:909)
Classical homocystinuria (Orphanet:394)
Cleft palate - short stature - vertebral anomalies (Orphanet:2015)
Cockayne syndrome (Orphanet:191)
Congenital contractural arachnodactyly (Orphanet:115)
Congenital muscular dystrophy due to LMNA mutation (Orphanet:157973)
Congenital unilateral hypoplasia of depressor anguli oris (Orphanet:1166)
Contractures - ectodermal dysplasia - cleft lip/palate (Orphanet:1484)
Cornelia de Lange syndrome (Orphanet:199)
Crane-Heise syndrome (Orphanet:1512)
Cranio-osteoarthropathy (Orphanet:1525)
Cryptorchidism - arachnodactyly - intellectual deficit (Orphanet:1548)
Cutis laxa-Marfanoid syndrome (Orphanet:171719)
Cyprus facial-neuromusculoskeletal syndrome (Orphanet:2674)
DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES (OMIM:127200)
Dermato-cardio-skeletal syndrome, Borrone type (Orphanet:1266)
Desmoid tumor (Orphanet:873)
Diastrophic dwarfism (Orphanet:628)
Digitotalar dysmorphism (Orphanet:1146)
Distal monosomy 10p (Orphanet:1580)
Distal symphalangism (Orphanet:3248)
Distal trisomy 15q (Orphanet:1707)
Dracunculiasis (Orphanet:231)
Duchenne and Becker muscular dystrophy (Orphanet:262)
Dyggve-Melchior-Clausen disease (Orphanet:239)
Dysmorphism - short stature - deafness - disorder of sex development (Orphanet:2282)
Dysplasia epiphysealis hemimelica (Orphanet:1822)
Dyssegmental dysplasia, Silverman-Handmaker type (Orphanet:1865)
Edinburgh malformation syndrome (Orphanet:1895)
Ehlers-Danlos syndrome, arthrochalasic type (Orphanet:1899)
Ehlers-Danlos syndrome, dermatosparaxis type (Orphanet:1901)
Ehlers-Danlos syndrome, hypermobility type (Orphanet:285)
Emery-Dreifuss muscular dystrophy (Orphanet:261)
Enchondromatosis (Orphanet:296)
Epidermolysis bullosa simplex with pyloric atresia (Orphanet:158684)
Extensor tendons of finger anomalies (Orphanet:3294)
Eye defects - arachnodactyly - cardiopathy (Orphanet:2725)
Familial Dupuytren contracture (Orphanet:79142)
Familial articular chondrocalcinosis (Orphanet:1416)
Familial symmetric lipomatosis (Orphanet:2398)
Familial visceral myopathy (Orphanet:2604)
Farber lipogranulomatosis (Orphanet:333)
Felty syndrome (Orphanet:47612)
Fetal akinesia deformation sequence (Orphanet:994)
Fetal alcohol syndrome (Orphanet:1915)
Fibrodysplasia ossificans progressiva (Orphanet:337)
Fibular aplasia - complex brachydactyly (Orphanet:2639)
Floating-Harbor syndrome (Orphanet:2044)
Flynn-Aird syndrome (Orphanet:2047)
Focal myositis (Orphanet:48918)
Freeman-Sheldon syndrome (Orphanet:2053)
Frontometaphyseal dysplasia (Orphanet:1826)
GELEOPHYSIC DYSPLASIA 2 (OMIM:614185)
GM1 gangliosidosis (Orphanet:354)
GM1 gangliosidosis type 1 (Orphanet:79255)
Gaucher disease (Orphanet:355)
Geleophysic dysplasia (Orphanet:2623)
Generalized congenital lipodystrophy with myopathy (Orphanet:228429)
German syndrome (Orphanet:2077)
Giant cell arteritis (Orphanet:397)
Glaucoma - ectopia - microspherophakia - stiff joints - short stature (Orphanet:2084)
Gordon syndrome (Orphanet:376)
Hall-Riggs syndrome (Orphanet:2107)
Harlequin ichthyosis (Orphanet:457)
Heart-hand syndrome type 2 (Orphanet:1350)
Hemochromatosis type 4 (Orphanet:139491)
Hereditary hyperekplexia (Orphanet:3197)
Holzgreve-Wagner-Rehder syndrome (Orphanet:2167)
Humero-radial synostosis (Orphanet:3265)
Humerus trochlea aplasia (Orphanet:3383)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hydrocephalus with stenosis of aqueduct of Sylvius (Orphanet:2182)
Hyperimmunoglobulinemia D with periodic fever (Orphanet:343)
Hypomyelination neuropathy - arthrogryposis (Orphanet:2680)
Hypophosphatemic rickets (Orphanet:437)
Hypoplastic tibiae - postaxial polydactyly (Orphanet:3332)
Hypospadias - intellectual deficit, Goldblatt type (Orphanet:2261)
IVIC syndrome (Orphanet:2307)
Infantile myofibromatosis (Orphanet:2591)
Intellectual deficit - balding - patella luxation - acromicria (Orphanet:3041)
Intellectual deficit - cataracts - calcified pinnae - myopathy (Orphanet:3042)
Intellectual deficit - myopathy - short stature - endocrine defect (Orphanet:3068)
Intellectual deficit, Wolff type (Orphanet:3080)
Intellectual disability-developmental delay-contractures syndrome (Orphanet:3454)
Isolated cloverleaf skull syndrome (Orphanet:2343)
Isolated ectopia lentis (Orphanet:1885)
Isolated osteopoikilosis (Orphanet:166119)
Junctional epidermolysis bullosa (Orphanet:305)
Juvenile dermatomyositis (Orphanet:93672)
Juvenile hyaline fibromatosis (Orphanet:2028)
Juvenile idiopathic arthritis (Orphanet:92)
Juvenile rheumatoid factor-negative polyarthritis (Orphanet:85408)
Juvenile rheumatoid factor-positive polyarthritis (Orphanet:85435)
KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS (OMIM:245160)
Kienbock disease (Orphanet:97332)
Kleefstra syndrome (Orphanet:261494)
Kniest dysplasia (Orphanet:485)
Kyphomelic dysplasia (Orphanet:1801)
Laurin-Sandrow syndrome (Orphanet:2378)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Leri pleonosteosis (Orphanet:2900)
Lethal congenital contracture syndrome type 1 (Orphanet:1486)
Lethal multiple pterygium syndrome (Orphanet:33108)
Lethal recessive chondrodysplasia (Orphanet:1423)
Lethal restrictive dermopathy (Orphanet:1662)
Lipodystrophy due to peptidic growth factors deficiency (Orphanet:1979)
Lowry-Wood syndrome (Orphanet:1824)
Léri-Weill dyschondrosteosis (Orphanet:240)
MUCOLIPIDOSIS III GAMMA (OMIM:252605)
Madelung deformity (Orphanet:35688)
Malignant hyperthermia - arthrogryposis - torticollis (Orphanet:2215)
Mandibuloacral dysplasia (Orphanet:2457)
Mandibuloacral dysplasia with type A lipodystrophy (Orphanet:90153)
Marden-Walker syndrome (Orphanet:2461)
Marfan syndrome (Orphanet:558)
Maternal hyperthermia induced birth defects (Orphanet:2216)
Melorheostosis (Orphanet:2485)
Mesomelia-synostoses syndrome (Orphanet:2496)
Mesomelic dwarfism, Nievergelt type (Orphanet:2633)
Metachromatic leukodystrophy (Orphanet:512)
Metaphyseal anadysplasia (Orphanet:1040)
Metaphyseal chondrodysplasia, Jansen type (Orphanet:33067)
Metatropic dysplasia (Orphanet:2635)
Micro syndrome (Orphanet:2510)
Microcephaly - cardiac defect - lung malsegmentation (Orphanet:2516)
Microcephaly - intellectual deficit - phalangeal and neurological anomalies (Orphanet:137658)
Microphthalmia - microtia - fetal akinesia (Orphanet:2547)
Mietens syndrome (Orphanet:2557)
Mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis (Orphanet:93279)
Mixed connective tissue disease (Orphanet:809)
Monosomy 9p (Orphanet:261112)
Morse-Rawnsley-Sargent syndrome (Orphanet:2570)
Mosaic trisomy 8 (Orphanet:96061)
Mosaic trisomy 9 (Orphanet:99776)
Mucolipidosis type 3 (Orphanet:577)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)
Mucopolysaccharidosis type 3 (Orphanet:581)
Mucopolysaccharidosis type 6 (Orphanet:583)
Mucopolysaccharidosis type 7 (Orphanet:584)
Multicentric carpo-tarsal osteolysis with or without nephropathy (Orphanet:2774)
Multifocal muscular fibrosis - obstructed vessels (Orphanet:2033)
Multiminicore myopathy (Orphanet:598)
Multiple epiphyseal dysplasia (Orphanet:251)
Multiple epiphyseal dysplasia due to collagen 9 anomaly (Orphanet:166002)
Multiple epiphyseal dysplasia type 1 (Orphanet:93308)
Multiple epiphyseal dysplasia type 5 (Orphanet:93311)
Multiple sulfatase deficiency (Orphanet:585)
Multiple synostoses syndrome (Orphanet:3237)
Mutilating palmoplantar keratoderma with periorificial keratotic plaques (Orphanet:659)
Myalgia-eosinophilia syndrome associated with tryptophan (Orphanet:2582)
Myhre syndrome (Orphanet:2588)
Myotonia permanens (Orphanet:99735)
Nager syndrome (Orphanet:245)
Nail-patella syndrome (Orphanet:2614)
Nakajo-Nishimura syndrome (Orphanet:2615)
Nasu-Hakola disease (Orphanet:2770)
Nephrogenic diabetes insipidus - intracranial calcification (Orphanet:3145)
Nestor-Guillermo progeria syndrome (Orphanet:280576)
Neurofibromatosis type 1 (Orphanet:636)
Neurogenic arthrogryposis multiplex congenita (Orphanet:1143)
Non-rhizomelic chondrodysplasia punctata (Orphanet:176)
OSLAM syndrome (Orphanet:2760)
OSTEOARTHRITIS SUSCEPTIBILITY 3 (OMIM:607850)
Oculocerebral hypopigmentation syndrome, Cross type (Orphanet:2719)
Oculocerebral hypopigmentation syndrome, Preus type (Orphanet:2720)
Oculocerebrorenal syndrome (Orphanet:534)
Ophthalmomandibulomelic dysplasia (Orphanet:2741)
Opsismodysplasia (Orphanet:2746)
Osteochondrodysplatic nanism - deafness - retinitis pigmentosa (Orphanet:2653)
Oto-onycho-peroneal syndrome (Orphanet:2793)
Otopalatodigital syndrome (Orphanet:669)
Otopalatodigital syndrome type 1 (Orphanet:90650)
Otospondylomegaepiphyseal dysplasia (Orphanet:1427)
PEHO syndrome (Orphanet:2836)
PHAVER syndrome (Orphanet:2876)
Pachydermoperiostosis (Orphanet:2796)
Parana hard-skin syndrome (Orphanet:2812)
Parastremmatic dwarfism (Orphanet:2646)
Pelizaeus-Merzbacher disease (Orphanet:702)
Pelvic dysplasia - arthrogryposis of lower limbs (Orphanet:2840)
Peripheral dysostosis (Orphanet:1795)
Peripheral motor neuropathy - dysautonomia (Orphanet:2400)
Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis (Orphanet:65288)
Pfeiffer syndrome type 2 (Orphanet:93259)
Pfeiffer syndrome type 3 (Orphanet:93260)
Pfeiffer-Palm-Teller syndrome (Orphanet:2871)
Pontocerebellar hypoplasia type 1 (Orphanet:2254)
Posterior fusion of lumbosacral vertebrae - blepharoptosis (Orphanet:2064)
Potassium-aggravated myotonia (Orphanet:612)
Progeria - short stature - pigmented nevi (Orphanet:2959)
Progressive non-infectious anterior vertebral fusion (Orphanet:2062)
Progressive osseous heteroplasia (Orphanet:2762)
Progressive pseudorheumatoid arthropathy of childhood (Orphanet:1159)
Proteus syndrome (Orphanet:744)
Proximal spinal muscular atrophy (Orphanet:70)
Pseudoachondroplasia (Orphanet:750)
Pyogenic arthritis - pyoderma gangrenosum - acne (Orphanet:69126)
Reactive arthritis (Orphanet:29207)
Relapsing polychondritis (Orphanet:728)
Renpenning syndrome (Orphanet:3242)
Rett syndrome (Orphanet:778)
Rhizomelic chondrodysplasia punctata (Orphanet:177)
Rhizomelic syndrome, Urbach type (Orphanet:3098)
Richards-Rundle syndrome (Orphanet:1399)
Rift valley fever (Orphanet:319251)
Rothmund-Thomson syndrome (Orphanet:2909)
STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET (OMIM:615934)
SYNDESMODYSPLASIC DWARFISM (OMIM:272450)
Sanfilippo syndrome type A (Orphanet:79269)
Sanfilippo syndrome type B (Orphanet:79270)
Sanfilippo syndrome type C (Orphanet:79271)
Sanfilippo syndrome type D (Orphanet:79272)
Say-Barber-Miller syndrome (Orphanet:3132)
Scheie syndrome (Orphanet:93474)
Schwartz-Jampel syndrome (Orphanet:800)
Self-healing collodion baby (Orphanet:281122)
Severe X-linked intellectual deficit, Gustavson type (Orphanet:3078)
Sheldon-Hall syndrome (Orphanet:1147)
Short stature - craniofacial anomalies - genital hypoplasia (Orphanet:2994)
Shoulder and thorax deformity - congenital heart disease (Orphanet:1940)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Sjögren-Larsson syndrome (Orphanet:816)
Smith-Magenis syndrome (Orphanet:819)
Spastic paraplegia type 2 (Orphanet:99015)
Spondylocarpotarsal synostosis (Orphanet:3275)
Spondyloepimetaphyseal dysplasia, Irapa type (Orphanet:93351)
Spondyloepimetaphyseal dysplasia, Missouri type (Orphanet:93356)
Spondyloepiphyseal dysplasia congenita (Orphanet:94068)
Spondylometaphyseal dysplasia - cone-rod dystrophy (Orphanet:85167)
Spondylometaphyseal dysplasia, A4 type (Orphanet:168555)
Spondylometaphyseal dysplasia, Kozlowski type (Orphanet:93314)
Spondyloperipheral dysplasia - short ulna (Orphanet:1856)
Stiff skin syndrome (Orphanet:2833)
Stoll-Alembik-Finck syndrome (Orphanet:3200)
Stüve-Wiedemann syndrome (Orphanet:3206)
Suarez-Stickler syndrome (Orphanet:166277)
Syndactyly type 4 (Orphanet:93405)
Thanatophoric dysplasia (Orphanet:2655)
Thanatophoric dysplasia type 1 (Orphanet:1860)
Thanatophoric dysplasia type 2 (Orphanet:93274)
Thiemann disease, familial form (Orphanet:3314)
Thumb stiffness - brachydactyly - intellectual deficit (Orphanet:1078)
Thymoma (Orphanet:99867)
Tibial aplasia - ectrodactyly (Orphanet:3329)
Torg-Winchester syndrome (Orphanet:3460)
Transgrediens et progrediens palmoplantar keratoderma (Orphanet:495)
Trismus - pseudocamptodactyly (Orphanet:3377)
Trisomy 17p (Orphanet:261290)
Trisomy 8q (Orphanet:1752)
Trisomy Xq28 (Orphanet:1762)
Ulna hypoplasia - intellectual deficit (Orphanet:2249)
Upington disease (Orphanet:3408)
Van den Ende-Gupta syndrome (Orphanet:2460)
Vici syndrome (Orphanet:1493)
WEILL-MARCHESANI SYNDROME 1 (OMIM:277600)
WEILL-MARCHESANI SYNDROME 3 (OMIM:614819)
Waardenburg syndrome type 3 (Orphanet:896)
Weaver syndrome (Orphanet:3447)
Weill-Marchesani syndrome (Orphanet:3449)
Werner syndrome (Orphanet:902)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)
Williams syndrome (Orphanet:904)
Wilson disease (Orphanet:905)
Wolfram syndrome (Orphanet:3463)
X-linked distal arthrogryposis multiplex congenita (Orphanet:1145)