Joint laxity
Symptom Information:
Symptom ID: | HPO:0001388 | |||||||||||||||||||||||
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) Joint laxity(HPO:0001388) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Joint disorders(MedDRA:10023213) Joint related disorders NEC(MedDRA:10027685) Joint laxity(HPO:0001388) |
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Database Frequency: | 117 / 7739 | |||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
15q24 microdeletion syndrome | (Orphanet:94065) |
48,XXYY syndrome | (Orphanet:10) |
ACHARD SYNDROME | (OMIM:100700) |
Acromesomelic dysplasia, Maroteaux type | (Orphanet:40) |
Aneurysm - osteoarthritis syndrome | (Orphanet:284984) |
Arterial tortuosity syndrome | (Orphanet:3342) |
Aspartylglucosaminuria | (Orphanet:93) |
Atkin-Flaitz syndrome | (Orphanet:1193) |
Autosomal dominant Larsen syndrome | (Orphanet:503) |
Autosomal recessive cutis laxa type 1 | (Orphanet:90349) |
BRITTLE CORNEA SYNDROME 1 | (OMIM:229200) |
BRUCK SYNDROME 1 | (OMIM:259450) |
Blepharophimosis-intellectual deficit syndrome, Ohdo type | (Orphanet:2728) |
Brittle cornea syndrome | (Orphanet:90354) |
Bruck syndrome | (Orphanet:2771) |
CATEL-MANZKE SYNDROME | (OMIM:616145) |
CLARK-BARAITSER SYNDROME | (OMIM:300602) |
COFFIN-SIRIS SYNDROME | (OMIM:135900) |
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA | (OMIM:219100) |
Cabezas syndrome | (Orphanet:85293) |
Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
Catel-Manzke syndrome | (Orphanet:1388) |
Cerebro-facio-articular syndrome | (Orphanet:314679) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Coffin-Siris syndrome | (Orphanet:1465) |
Congenital muscular dystrophy, Ullrich type | (Orphanet:75840) |
Costello syndrome | (Orphanet:3071) |
Cranioectodermal dysplasia | (Orphanet:1515) |
Cranioectodermal dysplasia 1 | (OMIM:218330) |
Cranioectodermal dysplasia 2 | (OMIM:613610) |
Cranioectodermal dysplasia 3 | (OMIM:614099) |
Craniofrontonasal dysplasia | (Orphanet:1520) |
Craniolenticulosutural dysplasia | (Orphanet:50814) |
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies | (Orphanet:221145) |
DESBUQUOIS DYSPLASIA 1 | (OMIM:251450) |
DESBUQUOIS DYSPLASIA 2 | (OMIM:615777) |
Desbuquois syndrome | (Orphanet:1425) |
Dislocation of the hip - dysmorphism | (Orphanet:2412) |
Down syndrome | (Orphanet:870) |
EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED | (OMIM:130090) |
EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE | (OMIM:608763) |
EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 1 | (OMIM:130070) |
EPIPHYSEAL DYSPLASIA, BAUMANN TYPE | (OMIM:610797) |
Ear-patella-short stature syndrome | (Orphanet:2554) |
Ehlers-Danlos syndrome type 11 | (Orphanet:2295) |
Ehlers-Danlos syndrome type 2 | (Orphanet:90318) |
Ehlers-Danlos syndrome, arthrochalasic type | (Orphanet:1899) |
Ehlers-Danlos syndrome, cardiac valvular type | (Orphanet:230851) |
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, musculocontractural type | (Orphanet:2953) |
Ehlers-Danlos syndrome, periodontitis type | (Orphanet:75392) |
Ehlers-Danlos syndrome, progeroid type | (Orphanet:75496) |
Ehlers-Danlos syndrome, spondylocheirodysplastic type | (Orphanet:157965) |
Floating-Harbor syndrome | (Orphanet:2044) |
Focal dermal hypoplasia | (Orphanet:2092) |
Fragile X syndrome | (Orphanet:908) |
HAJDU-CHENEY SYNDROME | (OMIM:102500) |
HELSMOORTEL-VAN DER AA SYNDROME | (OMIM:615873) |
HEMANGIOMATOSIS, CUTANEOUS, WITH ASSOCIATED FEATURES | (OMIM:234800) |
Hydrocephaly - tall stature - joint laxity | (Orphanet:2181) |
Hypospadias - intellectual deficit, Goldblatt type | (Orphanet:2261) |
Johanson-Blizzard syndrome | (Orphanet:2315) |
Joubert syndrome 18 | (OMIM:614815) |
Kaler-Garrity-Stern syndrome | (Orphanet:2324) |
LOEYS-DIETZ SYNDROME 1 | (OMIM:609192) |
LOEYS-DIETZ SYNDROME 2 | (OMIM:610168) |
LOEYS-DIETZ SYNDROME, TYPE 2A | (OMIM:608967) |
LUJAN-FRYNS SYNDROME | (OMIM:309520) |
Larsen-like osseous dysplasia - short stature | (Orphanet:2370) |
Larsen-like syndrome, B3GAT3 type | (Orphanet:284139) |
Loeys-Dietz syndrome type 1 | (Orphanet:60030) |
MACROEPIPHYSEAL DYSPLASIA WITH OSTEOPOROSIS, WRINKLED SKIN, AND AGEDAPPEARANCE | (OMIM:248010) |
MEIER-GORLIN SYNDROME 1 | (OMIM:224690) |
METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS | (OMIM:250460) |
MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM | (OMIM:616033) |
MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE | (OMIM:609456) |
Marfan syndrome type 2 | (Orphanet:284973) |
Megalencephaly-capillary malformation-polymicrogyria syndrome | (Orphanet:60040) |
Menkes disease | (Orphanet:565) |
Metaphyseal dysostosis - intellectual deficit - conductive deafness | (Orphanet:2502) |
Microcephaly - glomerulonephritis - marfanoid habitus | (Orphanet:2172) |
Monosomy 18q | (Orphanet:1600) |
Mucopolysaccharidosis type 4A | (Orphanet:309297) |
Mucopolysaccharidosis type 4B | (Orphanet:309310) |
Multiple endocrine neoplasia type 2B | (Orphanet:247709) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
OSTEOGENESIS IMPERFECTA, TYPE VIII | (OMIM:610915) |
OSTEOGENESIS IMPERFECTA, TYPE X | (OMIM:613848) |
OSTEOGENESIS IMPERFECTA, TYPE XI | (OMIM:610968) |
OSTEOGENESIS IMPERFECTA, TYPE XIII | (OMIM:614856) |
Occipital horn syndrome | (Orphanet:198) |
Perinatal lethal hypophosphatasia | (Orphanet:247623) |
Peters-plus syndrome | (Orphanet:709) |
Pseudoachondroplasia | (Orphanet:750) |
Renal coloboma syndrome | (Orphanet:1475) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |
SHORT syndrome | (Orphanet:3163) |
SOTOS SYNDROME 1 | (OMIM:117550) |
Shprintzen-Goldberg syndrome | (Orphanet:2462) |
Sotos syndrome | (Orphanet:821) |
Spondyloepimetaphyseal dysplasia with joint laxity | (Orphanet:93359) |
Spondyloepimetaphyseal dysplasia with multiple dislocations | (Orphanet:93360) |
Spondyloepimetaphyseal dysplasia, Shohat type | (Orphanet:93352) |
Spondyloepimetaphyseal dysplasia, aggrecan type | (Orphanet:171866) |
Spondyloepiphyseal dysplasia, Reardon type | (Orphanet:163662) |
Syndromic microphthalmia type 5 | (Orphanet:178364) |
TMEM165-CDG | (Orphanet:314667) |
VAN MALDERGEM SYNDROME 1 | (OMIM:601390) |
VAN MALDERGEM SYNDROME 2 | (OMIM:615546) |
WARBURG MICRO SYNDROME 1 | (OMIM:600118) |
Williams syndrome | (Orphanet:904) |
Wilson disease | (Orphanet:905) |
X-linked Ehlers-Danlos syndrome | (Orphanet:75497) |