Joint hypermobility
Symptom Information:
Symptom ID: | HPO:0001382 | |||||||||||||||||||||||
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 the skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal joint morphology(HPO:0001367) Abnormality of joint mobility(HPO:0011729) Joint hypermobility(HPO:0001382) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Joint disorders(MedDRA:10023213) Joint related disorders NEC(MedDRA:10027685) Joint hypermobility(HPO:0001382) |
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Database Frequency: | 231 / 7739 | |||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
10q22.3q23.3 microdeletion syndrome | (Orphanet:276413) |
15q11q13 microduplication syndrome | (Orphanet:238446) |
15q24 microdeletion syndrome | (Orphanet:94065) |
16p13.11 microduplication syndrome | (Orphanet:261243) |
17q11.2 microduplication syndrome | (Orphanet:139474) |
1q21.1 microdeletion syndrome | (Orphanet:250989) |
2q32q33 microdeletion syndrome | (Orphanet:251019) |
2q37 microdeletion syndrome | (Orphanet:1001) |
3M syndrome | (Orphanet:2616) |
3MC SYNDROME 2 | (OMIM:265050) |
3q29 microdeletion syndrome | (Orphanet:65286) |
48,XXXY syndrome | (Orphanet:96263) |
48,XXYY syndrome | (Orphanet:10) |
49,XXXXY syndrome | (Orphanet:96264) |
ALDH18A1-related De Barsy syndrome | (Orphanet:35664) |
Aarskog-Scott syndrome | (Orphanet:915) |
Achondroplasia | (Orphanet:15) |
Acrogeria | (Orphanet:2500) |
Acromegaloid facial appearance syndrome | (Orphanet:965) |
Acromesomelic dysplasia, Maroteaux type | (Orphanet:40) |
Acroosteolysis, dominant type | (Orphanet:955) |
Angel-shaped phalango-epiphyseal dysplasia | (Orphanet:63442) |
Arachnodactyly - abnormal ossification - intellectual deficit | (Orphanet:1129) |
Arachnodactyly - intellectual deficit - dysmorphism | (Orphanet:1130) |
Arterial tortuosity syndrome | (Orphanet:3342) |
Ataxia-deafness-retardation syndrome | (Orphanet:1188) |
Autosomal dominant Larsen syndrome | (Orphanet:503) |
Autosomal dominant cutis laxa | (Orphanet:90348) |
Autosomal dominant hyper-IgE syndrome | (Orphanet:2314) |
Autosomal recessive Stickler syndrome | (Orphanet:250984) |
Autosomal recessive cutis laxa type 1 | (Orphanet:90349) |
Autosomal recessive cutis laxa type 2 | (Orphanet:90350) |
Autosomal recessive cutis laxa type 2, classic type | (Orphanet:357074) |
Autosomal recessive cutis laxa type 2A | (Orphanet:357058) |
Autosomal recessive cutis laxa type 2B | (Orphanet:357064) |
Autosomal recessive facio-digito-genital syndrome | (Orphanet:1974) |
BRUCK SYNDROME 1 | (OMIM:259450) |
Bannayan-Riley-Ruvalcaba syndrome | (Orphanet:109) |
Bazex-Dupré-Christol syndrome | (Orphanet:113) |
Blepharonasofacial malformation syndrome | (Orphanet:1252) |
Blepharophimosis-intellectual deficit syndrome, MKB type | (Orphanet:293707) |
Blepharophimosis-intellectual deficit syndrome, Ohdo type | (Orphanet:2728) |
Blepharophimosis-intellectual deficit syndrome, SBBYS type | (Orphanet:3047) |
Bone dysplasia, lethal Holmgren type | (Orphanet:1842) |
Borjeson-Forssman-Lehmann syndrome | (Orphanet:127) |
Brachydactyly type E | (Orphanet:93387) |
Brachyolmia, Maroteaux type | (Orphanet:93302) |
Brittle cornea syndrome | (Orphanet:90354) |
CARDIOFACIOCUTANEOUS SYNDROME 1 | (OMIM:115150) |
CHARGE syndrome | (Orphanet:138) |
CK syndrome | (Orphanet:251383) |
CODAS syndrome | (Orphanet:1458) |
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB | (OMIM:614437) |
Cabezas syndrome | (Orphanet:85293) |
Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cartilage-hair hypoplasia | (Orphanet:175) |
Cataract - deafness - hypogonadism | (Orphanet:1383) |
Catel-Manzke syndrome | (Orphanet:1388) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Christianson syndrome | (Orphanet:85278) |
Cleft palate - short stature - vertebral anomalies | (Orphanet:2015) |
Coffin-Lowry syndrome | (Orphanet:192) |
Coffin-Siris syndrome | (Orphanet:1465) |
Cohen syndrome | (Orphanet:193) |
Cole-Carpenter syndrome | (Orphanet:2050) |
Congenital muscular dystrophy - infantile cataract - hypogonadism | (Orphanet:1875) |
Congenital muscular dystrophy due to LMNA mutation | (Orphanet:157973) |
Congenital osteogenesis imperfecta - microcephaly - cataracts | (Orphanet:2772) |
Cooper-Jabs syndrome | (Orphanet:1488) |
Costello syndrome | (Orphanet:3071) |
Cranioectodermal dysplasia | (Orphanet:1515) |
Cranioectodermal dysplasia 4 | (OMIM:614378) |
Craniofaciofrontodigital syndrome | (Orphanet:363705) |
Craniofrontonasal dysplasia | (Orphanet:1520) |
Craniolenticulosutural dysplasia | (Orphanet:50814) |
De Barsy syndrome | (Orphanet:2962) |
Desbuquois syndrome | (Orphanet:1425) |
Diastrophic dwarfism | (Orphanet:628) |
Dislocation of the hip - dysmorphism | (Orphanet:2412) |
Distal 22q11.2 microdeletion syndrome | (Orphanet:261330) |
Distal monosomy 19p13.3 | (Orphanet:96129) |
Down syndrome | (Orphanet:870) |
Dubowitz syndrome | (Orphanet:235) |
Dysmorphism - pectus carinatum - joint laxity | (Orphanet:2104) |
EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE | (OMIM:608763) |
Ear-patella-short stature syndrome | (Orphanet:2554) |
Ehlers-Danlos syndrome due to tenascin-X deficiency | (Orphanet:230839) |
Ehlers-Danlos syndrome type 1 | (Orphanet:90309) |
Ehlers-Danlos syndrome type 11 | (Orphanet:2295) |
Ehlers-Danlos syndrome type 2 | (Orphanet:90318) |
Ehlers-Danlos syndrome type 7A | (Orphanet:99875) |
Ehlers-Danlos syndrome type 7B | (Orphanet:99876) |
Ehlers-Danlos syndrome with periventricular heterotopia | (Orphanet:82004) |
Ehlers-Danlos syndrome, arthrochalasic type | (Orphanet:1899) |
Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
Ehlers-Danlos syndrome, dermatosparaxis type | (Orphanet:1901) |
Ehlers-Danlos syndrome, fibronectinemic type | (Orphanet:75501) |
Ehlers-Danlos syndrome, hypermobility type | (Orphanet:285) |
Ehlers-Danlos syndrome, kyphoscoliotic type | (Orphanet:1900) |
Ehlers-Danlos syndrome, periodontitis type | (Orphanet:75392) |
Ehlers-Danlos syndrome, progeroid type | (Orphanet:75496) |
Ehlers-Danlos syndrome, spondylocheirodysplastic type | (Orphanet:157965) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
Encephalopathy due to beta-mercaptolactate-cysteine disulfiduria | (Orphanet:1035) |
Facial dysmorphism - shawl scrotum - joint laxity | (Orphanet:1778) |
Floating-Harbor syndrome | (Orphanet:2044) |
Fragile X syndrome | (Orphanet:908) |
Fried syndrome | (Orphanet:85335) |
Fryns-Smeets-Thiry syndrome | (Orphanet:2058) |
GAPO syndrome | (Orphanet:2067) |
Geroderma osteodysplastica | (Orphanet:2078) |
Goldblatt syndrome | (Orphanet:166272) |
Grant syndrome | (Orphanet:2097) |
Hallermann-Streiff syndrome | (Orphanet:2108) |
Harrod syndrome | (Orphanet:2115) |
Hereditary acrokeratotic poikiloderma, Weary type | (Orphanet:2907) |
Holoprosencephaly | (Orphanet:2162) |
Hydrocephaly - tall stature - joint laxity | (Orphanet:2181) |
Hypertrichosis cubiti - short stature | (Orphanet:2220) |
Hypertryptophanemia | (Orphanet:2224) |
Hypochondroplasia | (Orphanet:429) |
Imperforate oropharynx - costo vetebral anomalies | (Orphanet:2759) |
Intellectual deficit - balding - patella luxation - acromicria | (Orphanet:3041) |
Intellectual deficit, X-linked - seizures - psoriasis | (Orphanet:3052) |
Intellectual deficit, X-linked, Miles-Carpenter type | (Orphanet:85283) |
KABUKI SYNDROME 1 | (OMIM:147920) |
Kabuki syndrome | (Orphanet:2322) |
Kaler-Garrity-Stern syndrome | (Orphanet:2324) |
Knobloch syndrome | (Orphanet:1571) |
Koolen-De Vries syndrome | (Orphanet:96169) |
LOEYS-DIETZ SYNDROME, TYPE 2A | (OMIM:608967) |
Langer-Giedion syndrome | (Orphanet:502) |
Larsen-like osseous dysplasia - short stature | (Orphanet:2370) |
Lateral meningocele syndrome | (Orphanet:2789) |
Lenz-Majewski hyperostotic dwarfism | (Orphanet:2658) |
Lethal recessive chondrodysplasia | (Orphanet:1423) |
Loeys-Dietz syndrome type 1 | (Orphanet:60030) |
Low birth weight - dwarfism - dysgammaglobulinemia | (Orphanet:2621) |
MACS syndrome | (Orphanet:217335) |
MARFANOID HYPERMOBILITY SYNDROME | (OMIM:154750) |
MEIER-GORLIN SYNDROME 2 | (OMIM:613800) |
MENTAL RETARDATION, X-LINKED 21 | (OMIM:300143) |
MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES | (OMIM:607597) |
Marfan syndrome | (Orphanet:558) |
Marfan syndrome type 1 | (Orphanet:284963) |
Marshall-Smith syndrome | (Orphanet:561) |
Megalencephaly-capillary malformation-polymicrogyria syndrome | (Orphanet:60040) |
Megalocornea-intellectual deficit syndrome | (Orphanet:2479) |
Menkes disease | (Orphanet:565) |
Micro syndrome | (Orphanet:2510) |
Microcephalic osteodysplastic primordial dwarfism type 2 | (Orphanet:2637) |
Microcephaly - brachydactyly - kyphoscoliosis | (Orphanet:3433) |
Microcephaly - glomerulonephritis - marfanoid habitus | (Orphanet:2172) |
Monosomy 5p | (Orphanet:281) |
Monosomy 9q22.3 | (Orphanet:77301) |
Mucopolysaccharidosis type 4 | (Orphanet:582) |
Multiminicore myopathy | (Orphanet:598) |
Multiple endocrine neoplasia type 2 | (Orphanet:653) |
NEMALINE MYOPATHY 7 | (OMIM:610687) |
Nail-patella syndrome | (Orphanet:2614) |
Neuhauser-Eichner-Opitz syndrome | (Orphanet:2672) |
Night blindness - skeletal anomalies - dysmorphism | (Orphanet:1390) |
Non-distal trisomy 10q | (Orphanet:1695) |
Noonan syndrome | (Orphanet:648) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
OSTEOGENESIS IMPERFECTA, TYPE XIII | (OMIM:614856) |
Occipital horn syndrome | (Orphanet:198) |
Oculo-palato-cerebral syndrome | (Orphanet:2714) |
Oculo-reno-cerebellar syndrome | (Orphanet:2715) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Osteodysplasty, Melnick-Needles type | (Orphanet:2484) |
Osteogenesis imperfecta | (Orphanet:666) |
Osteogenesis imperfecta type 1 | (Orphanet:216796) |
Osteogenesis imperfecta type 5 | (Orphanet:216828) |
Osteoporosis - macrocephaly - blindness - joint hyperlaxity | (Orphanet:2787) |
Osteoporosis - pseudoglioma | (Orphanet:2788) |
PIERRE ROBIN SEQUENCE WITH PECTUS EXCAVATUM AND RIB AND SCAPULAR ANOMALIES | (OMIM:602196) |
Paraplegia - intellectual deficit - hyperkeratosis | (Orphanet:2824) |
Peters-plus syndrome | (Orphanet:709) |
Pili torti - developmental delay - neurological abnormalities | (Orphanet:2891) |
Polyvalvular heart disease syndrome | (Orphanet:228410) |
Pseudoachondroplasia | (Orphanet:750) |
Pseudoxanthoma elasticum | (Orphanet:758) |
Pterygium colli - intellectual deficit - digital anomalies | (Orphanet:2988) |
RAPADILINO syndrome | (Orphanet:3021) |
RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION | (OMIM:268050) |
RIENHOFF SYNDROME | (OMIM:615582) |
Renal coloboma syndrome | (Orphanet:1475) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Renal tubular dysgenesis | (Orphanet:3033) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
Rubinstein-Taybi syndrome | (Orphanet:783) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |
SCARF syndrome | (Orphanet:3134) |
SHORT syndrome | (Orphanet:3163) |
SPONASTRIME dysplasia | (Orphanet:93357) |
Sakati-Nyhan syndrome | (Orphanet:3128) |
Seckel syndrome | (Orphanet:808) |
Short stature - valvular heart disease - characteristic facies | (Orphanet:2868) |
Shprintzen-Goldberg syndrome | (Orphanet:2462) |
Spinocerebellar ataxia - dysmorphism | (Orphanet:1185) |
Spondylo-ocular syndrome | (Orphanet:85194) |
Spondyloepimetaphyseal dysplasia with joint laxity | (Orphanet:93359) |
Spondyloepimetaphyseal dysplasia with multiple dislocations | (Orphanet:93360) |
Spondyloepimetaphyseal dysplasia, Shohat type | (Orphanet:93352) |
Stickler syndrome | (Orphanet:828) |
Stickler syndrome type 1 | (Orphanet:90653) |
Stickler syndrome type 2 | (Orphanet:90654) |
TEMPLE SYNDROME | (OMIM:616222) |
THREE M SYNDROME 1 | (OMIM:273750) |
Tel Hashomer camptodactyly syndrome | (Orphanet:3292) |
Temtamy syndrome | (Orphanet:1777) |
Tetrasomy 12p | (Orphanet:884) |
Tetrasomy X | (Orphanet:9) |
Thanatophoric dysplasia | (Orphanet:2655) |
Thoracomelic dysplasia | (Orphanet:1803) |
Trisomy 20p | (Orphanet:261318) |
Trisomy X | (Orphanet:3375) |
VESICOURETERAL REFLUX 8 | (OMIM:615963) |
WARBURG MICRO SYNDROME 1 | (OMIM:600118) |
Weaver syndrome | (Orphanet:3447) |
White forelock with malformations | (Orphanet:2475) |
Williams syndrome | (Orphanet:904) |
Wilson disease | (Orphanet:905) |
Wrinkly skin syndrome | (Orphanet:2834) |
X-linked Ehlers-Danlos syndrome | (Orphanet:75497) |
X-linked creatine transporter deficiency | (Orphanet:52503) |
X-linked intellectual deficit with marfanoid habitus | (Orphanet:776) |
Zimmermann-Laband syndrome | (Orphanet:3473) |