以 HPO 交叉檢視

HPO → 對應的病歷用詞，並附加具此 HPO 的疾病作為參考。

搜尋 HPO

Limitation of joint mobility

HP:0001376

對應病歷用詞(0)

尚無對應用詞。

具此 HPO 的疾病（附加參考）(118)

Arginine vasopressin resistance-intracranial calcification-short stature-facial dysmorphism syndromeORPHA:3145 · Very frequent (99-80%)
Atypical Werner syndromeORPHA:79474 · Very frequent (99-80%)
Autosomal recessive multiple pterygium syndromeORPHA:2990 · Very frequent (99-80%)
Blau syndromeORPHA:90340 · Very frequent (99-80%)
Contractures-ectodermal dysplasia-cleft lip/palate syndromeORPHA:1484 · Very frequent (99-80%)
Cutis laxa-Marfanoid syndromeORPHA:171719 · Very frequent (99-80%)
Felty syndromeORPHA:47612 · Very frequent (99-80%)
Fibrodysplasia ossificans progressivaORPHA:337 · Very frequent (99-80%)
Fibular aplasia-complex brachydactyly syndromeORPHA:2639 · Very frequent (99-80%)
German syndromeORPHA:2077 · Very frequent (99-80%)
Hurler syndromeORPHA:93473 · Very frequent (99-80%)
Hurler-Scheie syndromeORPHA:93476 · Very frequent (99-80%)
Hypomyelination neuropathy-arthrogryposis syndromeORPHA:2680 · Very frequent (99-80%)
Intellectual disability, Wolff typeORPHA:3080 · Very frequent (99-80%)
Isolated humero-radial synostosisORPHA:3265 · Very frequent (99-80%)
Kagami-Ogata syndromeORPHA:254519 · Very frequent (99-80%)
Kienbock diseaseORPHA:97332 · Very frequent (99-80%)
Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndromeORPHA:2570 · Very frequent (99-80%)
Mandibuloacral dysplasia with type A lipodystrophyORPHA:90153 · Very frequent (99-80%)
Mesomelic dysplasia, Nievergelt typeORPHA:2633 · Very frequent (99-80%)
Microphthalmia-microtia-fetal akinesia syndromeORPHA:2547 · Very frequent (99-80%)
Microtriplication 11q24.1 syndromeORPHA:289522 · Very frequent (99-80%)
Mucopolysaccharidosis type 2ORPHA:580 · Very frequent (99-80%)
Multicentric carpo-tarsal osteolysis with or without nephropathyORPHA:2774 · Very frequent (99-80%)
Nasu-Hakola diseaseORPHA:2770 · Very frequent (99-80%)
Ophthalmomandibulomelic dysplasiaORPHA:2741 · Very frequent (99-80%)
Osteochondritis dissecansORPHA:2764 · Very frequent (99-80%)
Otopalatodigital syndrome type 1ORPHA:90650 · Very frequent (99-80%)
PAPA syndromeORPHA:69126 · Very frequent (99-80%)
Pelvic dysplasia-arthrogryposis of lower limbs syndromeORPHA:2840 · Very frequent (99-80%)
Pfeiffer syndrome type 2ORPHA:93259 · Very frequent (99-80%)
Pfeiffer syndrome type 3ORPHA:93260 · Very frequent (99-80%)
Progressive osseous heteroplasiaORPHA:2762 · Very frequent (99-80%)
Rhizomelic syndrome, Urbach typeORPHA:3098 · Very frequent (99-80%)
Scheie syndromeORPHA:93474 · Very frequent (99-80%)
Self-improving collodion babyORPHA:281122 · Very frequent (99-80%)
Spondyloepimetaphyseal dysplasia, Irapa typeORPHA:93351 · Very frequent (99-80%)
Stiff skin syndromeORPHA:2833 · Very frequent (99-80%)
Trismus-pseudocamptodactyly syndromeORPHA:3377 · Very frequent (99-80%)
Wieacker-Wolff syndromeORPHA:3454 · Very frequent (99-80%)
8q22.1 microdeletion syndromeORPHA:178303 · Frequent (79-30%)
Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndromeORPHA:1192 · Frequent (79-30%)
Atypical teratoid rhabdoid tumorORPHA:99966 · Frequent (79-30%)
Aymé-Gripp syndromeORPHA:1272 · Frequent (79-30%)
Bohring-Opitz syndromeORPHA:97297 · Frequent (79-30%)
Brachydactylous dwarfism, Mseleni typeORPHA:2619 · Frequent (79-30%)
C syndromeORPHA:1308 · Frequent (79-30%)
Camurati-Engelmann diseaseORPHA:1328 · Frequent (79-30%)
Congenital muscular dystrophy due to LMNA mutationORPHA:157973 · Frequent (79-30%)
Crisponi syndromeORPHA:1545 · Frequent (79-30%)
DracunculiasisORPHA:231 · Frequent (79-30%)
Dyssegmental dysplasia, Silverman-Handmaker typeORPHA:1865 · Frequent (79-30%)
Extensor tendons of finger anomaliesORPHA:3294 · Frequent (79-30%)
Filippi syndromeORPHA:3255 · Frequent (79-30%)
Geleophysic dysplasiaORPHA:2623 · Frequent (79-30%)
Harlequin ichthyosisORPHA:457 · Frequent (79-30%)
Hutchinson-Gilford progeria syndromeORPHA:740 · Frequent (79-30%)
Intellectual disability-myopathy-short stature-endocrine defect syndromeORPHA:3068 · Frequent (79-30%)
Kyphomelic dysplasiaORPHA:1801 · Frequent (79-30%)
Laurin-Sandrow syndromeORPHA:2378 · Frequent (79-30%)
Lethal congenital contracture syndrome type 1ORPHA:1486 · Frequent (79-30%)
Monosomy 9p syndromeORPHA:261112 · Frequent (79-30%)
Mosaic trisomy 8 syndromeORPHA:96061 · Frequent (79-30%)
Mosaic trisomy 9 syndromeORPHA:99776 · Frequent (79-30%)
Mucolipidosis type IIORPHA:576 · Frequent (79-30%)
Multiple epiphyseal dysplasia type 4ORPHA:93307 · Frequent (79-30%)
Multiple osteochondromasORPHA:321 · Frequent (79-30%)
Myalgia-eosinophilia syndrome associated with tryptophanORPHA:2582 · Frequent (79-30%)
Oculocerebral hypopigmentation syndrome, Cross typeORPHA:2719 · Frequent (79-30%)
PachydermoperiostosisORPHA:2796 · Frequent (79-30%)
PEHO syndromeORPHA:2836 · Frequent (79-30%)
Progressive pseudorheumatoid dysplasiaORPHA:1159 · Frequent (79-30%)
Relapsing polychondritisORPHA:728 · Frequent (79-30%)
Rheumatoid factor-positive polyarticular juvenile idiopathic arthritisORPHA:85435 · Frequent (79-30%)
Rhizomelic chondrodysplasia punctataORPHA:177 · Frequent (79-30%)
Secondary non-traumatic avascular necrosisORPHA:399180 · Frequent (79-30%)
Short stature-craniofacial anomalies-genital hypoplasia syndromeORPHA:2994 · Frequent (79-30%)
Spondyloepiphyseal dysplasia tardaORPHA:93284 · Frequent (79-30%)
Spondylometaphyseal dysplasia, 'corner fracture' typeORPHA:93315 · Frequent (79-30%)
Stüve-Wiedemann syndromeORPHA:3206 · Frequent (79-30%)
Tenosynovial giant cell tumorORPHA:66627 · Frequent (79-30%)
Thiemann disease, familial formORPHA:3314 · Frequent (79-30%)
Tibial aplasia-ectrodactyly syndromeORPHA:3329 · Frequent (79-30%)
Weill-Marchesani syndromeORPHA:3449 · Frequent (79-30%)
17q23.1q23.2 microdeletion syndromeORPHA:261279 · Occasional (29-5%)
Adult polyglucosan body diseaseORPHA:206583 · Occasional (29-5%)
ALG1-CDGORPHA:79327 · Occasional (29-5%)
Amish lethal microcephalyORPHA:99742 · Occasional (29-5%)
Autosomal recessive otospondylomegaepiphyseal dysplasiaORPHA:1427 · Occasional (29-5%)
BabesiosisORPHA:108 · Occasional (29-5%)
Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiencyORPHA:95699 · Occasional (29-5%)
Desmoid tumorORPHA:873 · Occasional (29-5%)
Familial calcium pyrophosphate depositionORPHA:1416 · Occasional (29-5%)
Focal myositisORPHA:48918 · Occasional (29-5%)
Gordon syndromeORPHA:376 · Occasional (29-5%)
Hyperimmunoglobulinemia D with periodic feverORPHA:343 · Occasional (29-5%)
Hypermobile Ehlers-Danlos syndromeORPHA:285 · Occasional (29-5%)
Infantile myofibromatosisORPHA:2591 · Occasional (29-5%)
Intellectual disability-strabismus syndromeORPHA:363528 · Occasional (29-5%)
Isolated fibular hemimeliaORPHA:93323 · Occasional (29-5%)
Isolated osteopoikilosisORPHA:166119 · Occasional (29-5%)
Juvenile dermatomyositisORPHA:93672 · Occasional (29-5%)
Kleefstra syndromeORPHA:261494 · Occasional (29-5%)
Lenz-Majewski hyperostotic dysplasiaORPHA:2658 · Occasional (29-5%)
Megalencephaly-severe kyphoscoliosis-overgrowth syndromeORPHA:457359 · Occasional (29-5%)
Moderate hemophilia AORPHA:169805 · Occasional (29-5%)
Multiple epiphyseal dysplasia type 1ORPHA:93308 · Occasional (29-5%)
Myotonia permanensORPHA:99735 · Occasional (29-5%)
Psoriasis-related juvenile idiopathic arthritisORPHA:85436 · Occasional (29-5%)
Severe hemophilia AORPHA:169802 · Occasional (29-5%)
Spastic paraplegia type 2ORPHA:99015 · Occasional (29-5%)
Spondylometaphyseal dysplasia, A4 typeORPHA:168555 · Occasional (29-5%)
Syndactyly type 4ORPHA:93405 · Occasional (29-5%)
Thanatophoric dysplasia type 2ORPHA:93274 · Occasional (29-5%)
Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasiaORPHA:166277 · Occasional (29-5%)
X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disabilityORPHA:480880 · Occasional (29-5%)
X-linked hypophosphatemiaORPHA:89936 · Occasional (29-5%)
Richieri Costa-da Silva syndromeORPHA:3101 · Excluded (0%)