Hip dysplasia

Symptom Information:

Symptom ID: HPO:0001385
Synonyms:
Congenital hip dysplasia [HPO:0001385]
Hip dysplasia [Orphanet:46600]
Congenital hip dysplasia [OMIM:Congenital hip dysplasia]
Hip dysplasia [OMIM:Hip dysplasia]
Hip dislocation/dysplasia/coxa valga/coxa vara/coxa plana [Orphanet:46600]
Developmental hip dysplasia [MedDRA:10073767]
Acetabular dysplasia [MedDRA:10073767]
Clicking hip (suspected cong. disloc. of hip) [MedDRA:10073767]
Congenital dislocation of hip [MedDRA:10073767]
Congenital dislocation of hip, bilateral [MedDRA:10073767]
Congenital dislocation of hip, unilateral [MedDRA:10073767]
Congenital dislocation of one hip with subluxation of other hip [MedDRA:10073767]
Congenital hip deformity NOS [MedDRA:10073767]
Congenital hip dislocation [MedDRA:10073767]
Congenital subluxation of hip, bilateral [MedDRA:10073767]
Congenital subluxation of hip, unilateral [MedDRA:10073767]
Coxa valga, congenital [MedDRA:10073767]
Coxa vara, congenital [MedDRA:10073767]
Dislocation of hip congenital [MedDRA:10073767]
Other congenital deformity of hip (joint) [MedDRA:10073767]
Congenital hip deformity [MedDRA:10073767]
Hip dysplasia [MedDRA:10073767]
Acetabular dysplasia (rare) [OMIM:Acetabular dysplasia (rare)]
Congenital hip dislocation (rare) [OMIM:Congenital hip dislocation (rare)]
Hip dysplasia (in some patients) [OMIM:Hip dysplasia (in some patients)]
Hip dysplasia (reported in 2 patients) [OMIM:Hip dysplasia (reported in 2 patients)]
Quality:
Cross references:
Orphanet:46600 "Hip dislocation/dysplasia/coxa valga/coxa vara/coxa plana" [Orphanet:46600]
OMIM: "Congenital hip dysplasia" [OMIM:Congenital hip dysplasia]
OMIM: "Hip dysplasia" [OMIM:Hip dysplasia]
OMIM: "Acetabular dysplasia (rare)" [OMIM:Acetabular dysplasia (rare)]
OMIM: "Congenital hip dislocation (rare)" [OMIM:Congenital hip dislocation (rare)]
OMIM: "Hip dysplasia (in some patients)" [OMIM:Hip dysplasia (in some patients)]
OMIM: "Hip dysplasia (reported in 2 patients)" [OMIM:Hip dysplasia (reported in 2 patients)]
UMLS:C1328407 "Hip dysplasia" [Orphanet:46600]
Is a (Direct Parents):
MedDRA Musculoskeletal and connective tissue disorders of limbs congenital
HPO         Abnormality of the hip bone
Orphanet Joint dislocation
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 appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the lower limb(HPO:0002814)
                      Abnormality of lower limb joint(HPO:0100491)
                         Abnormality of the hip bone(HPO:0003272)
                            Hip dysplasia(HPO:0001385)
                Abnormality of pelvic girdle bone morphology(HPO:0002644)
                   Abnormality of the hip bone(HPO:0003272)
                      Hip dysplasia(HPO:0001385)
             Abnormal joint morphology(HPO:0001367)
                Abnormality of lower limb joint(HPO:0100491)
                   Abnormality of the hip bone(HPO:0003272)
                      Hip dysplasia(HPO:0001385)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396)
       Musculoskeletal and connective tissue disorders of limbs congenital(MedDRA:10028381)
          Hip dysplasia(HPO:0001385)
Database Frequency: 242 / 7739
Resource:

All diseases associated with this symptom:

16q24.3 microdeletion syndrome (Orphanet:261250)
17p13.3 microduplication syndrome (Orphanet:217385)
17q23.1q23.2 microdeletion syndrome (Orphanet:261279)
19q13.11 microdeletion syndrome (Orphanet:217346)
1p36 deletion syndrome (Orphanet:1606)
1q21.1 microduplication syndrome (Orphanet:250994)
2q23.1 microdeletion syndrome (Orphanet:228402)
3C syndrome (Orphanet:7)
3M syndrome (Orphanet:2616)
48,XXXY syndrome (Orphanet:96263)
48,XXYY syndrome (Orphanet:10)
49,XXXXY syndrome (Orphanet:96264)
ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM,AND TRACHEAL STENOSIS (OMIM:601427)
ARTERIOSCLEROSIS, SEVERE JUVENILE (OMIM:208060)
ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2 (OMIM:613404)
Aase-Smith syndrome (Orphanet:916)
Acro-renal-mandibular syndrome (Orphanet:958)
Acrocapitofemoral dysplasia (Orphanet:63446)
Acrocraniofacial dysostosis (Orphanet:949)
Acromesomelic dysplasia, Hunter-Thomson type (Orphanet:968)
Aicardi syndrome (Orphanet:50)
Albright hereditary osteodystrophy (Orphanet:665)
Alopecia - contractures - dwarfism - intellectual deficit (Orphanet:1005)
Alpha-mannosidosis (Orphanet:61)
Angel-shaped phalango-epiphyseal dysplasia (Orphanet:63442)
Aortic arch anomaly - peculiar facies - intellectual deficit (Orphanet:1110)
Arterial tortuosity syndrome (Orphanet:3342)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
Arthrogryposis due to muscular dystrophy (Orphanet:1155)
Arthrogryposis multiplex congenita (Orphanet:1037)
Auriculoosteodysplasia (Orphanet:114)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures (Orphanet:363454)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive cutis laxa type 2 (Orphanet:90350)
Autosomal recessive limb-girdle muscular dystrophy type 2S (Orphanet:369840)
Axial spondylometaphyseal dysplasia (Orphanet:168549)
Borjeson-Forssman-Lehmann syndrome (Orphanet:127)
Brachydactylous dwarfism, Mseleni type (Orphanet:2619)
Brittle cornea syndrome (Orphanet:90354)
CHARGE syndrome (Orphanet:138)
CODAS syndrome (Orphanet:1458)
Campomelic dysplasia (Orphanet:140)
Camptodactyly - joint contractures - facial skeletal defects (Orphanet:1323)
Camptodactyly syndrome, Guadalajara type 2 (Orphanet:1326)
Camurati-Engelmann disease (Orphanet:1328)
Cartilage-hair hypoplasia (Orphanet:175)
Cat-eye syndrome (Orphanet:195)
Cenani-Lenz syndrome (Orphanet:3258)
Cleft lip/palate - deafness - sacral lipoma (Orphanet:2003)
Cleft palate - short stature - vertebral anomalies (Orphanet:2015)
Cloacal exstrophy (Orphanet:93929)
Coffin-Siris syndrome (Orphanet:1465)
Cohen syndrome (Orphanet:193)
Conductive deafness - ptosis - skeletal anomalies (Orphanet:3236)
Congenital unilateral hypoplasia of depressor anguli oris (Orphanet:1166)
Cooper-Jabs syndrome (Orphanet:1488)
Cornelia de Lange syndrome (Orphanet:199)
Costello syndrome (Orphanet:3071)
Coxo-podo-patellar syndrome (Orphanet:1509)
Coxoauricular syndrome (Orphanet:1508)
Cranioectodermal dysplasia 4 (OMIM:614378)
Craniofacial dysplasia-osteopenia syndrome (Orphanet:314555)
Craniofaciofrontodigital syndrome (Orphanet:363705)
Cutis laxa (Orphanet:209)
Cutis laxa-Marfanoid syndrome (Orphanet:171719)
Cyprus facial-neuromusculoskeletal syndrome (Orphanet:2674)
De Barsy syndrome (Orphanet:2962)
Deafness - genital anomalies - metacarpal and metatarsal synostosis (Orphanet:3224)
Desbuquois syndrome (Orphanet:1425)
Developmental malformations - deafness - dystonia (Orphanet:79107)
Diastrophic dwarfism (Orphanet:628)
Digitotalar dysmorphism (Orphanet:1146)
Dislocation of the hip - dysmorphism (Orphanet:2412)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Distal monosomy 17q (Orphanet:1597)
Distal monosomy 6p (Orphanet:96125)
Dyggve-Melchior-Clausen disease (Orphanet:239)
Ehlers-Danlos syndrome type 11 (Orphanet:2295)
Ehlers-Danlos syndrome, arthrochalasic type (Orphanet:1899)
Ehlers-Danlos syndrome, dermatosparaxis type (Orphanet:1901)
Ehlers-Danlos syndrome, hypermobility type (Orphanet:285)
Ehlers-Danlos syndrome, kyphoscoliotic type (Orphanet:1900)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Epimetaphyseal skeletal dysplasia (Orphanet:1819)
Eye defects - arachnodactyly - cardiopathy (Orphanet:2725)
Familial clubfoot due to 17q23.1q23.2 microduplication (Orphanet:238578)
Fanconi anemia (Orphanet:84)
Femoral-facial syndrome (Orphanet:1988)
Fibular aplasia - complex brachydactyly (Orphanet:2639)
Frank-Ter Haar syndrome (Orphanet:137834)
Fryns-Smeets-Thiry syndrome (Orphanet:2058)
Fuhrmann syndrome (Orphanet:2854)
Geroderma osteodysplastica (Orphanet:2078)
Goldblatt syndrome (Orphanet:166272)
Hereditary acrokeratotic poikiloderma, Weary type (Orphanet:2907)
Hereditary hyperekplexia (Orphanet:3197)
Hereditary orotic aciduria (Orphanet:30)
Hereditary sensory and autonomic neuropathy type 2 (Orphanet:970)
Hermansky-Pudlak syndrome with neutropenia (Orphanet:183678)
Hip dysplasia, Beukes type (Orphanet:2114)
Hirsutism - skeletal dysplasia - intellectual deficit (Orphanet:2156)
Holoprosencephaly - craniosynostosis (Orphanet:2163)
Humerus trochlea aplasia (Orphanet:3383)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hutchinson-Gilford progeria syndrome (Orphanet:740)
Hydrocephalus - blue sclerae - nephropathy (Orphanet:2186)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
Hypertryptophanemia (Orphanet:2224)
Hypocalcemic vitamin D-resistant rickets (Orphanet:93160)
Intellectual deficit - cataracts - calcified pinnae - myopathy (Orphanet:3042)
Intellectual deficit - myopathy - short stature - endocrine defect (Orphanet:3068)
Intellectual deficit - spasticity - ectrodactyly (Orphanet:1891)
Intellectual deficit, X-linked - dysmorphism - cerebral atrophy (Orphanet:2958)
Isolated sedoheptulokinase deficiency (ORPHA:440713)
Isolated spina bifida (Orphanet:823)
Jacobsen syndrome (Orphanet:2308)
Kabuki syndrome (Orphanet:2322)
Kniest dysplasia (Orphanet:485)
Koolen-De Vries syndrome (Orphanet:96169)
Langer-Giedion syndrome (Orphanet:502)
Larsen-like osseous dysplasia - short stature (Orphanet:2370)
Lethal Larsen-like syndrome (Orphanet:2371)
Lethal congenital contracture syndrome type 1 (Orphanet:1486)
Lowry-Wood syndrome (Orphanet:1824)
Léri-Weill dyschondrosteosis (Orphanet:240)
MELAS (Orphanet:550)
Marden-Walker syndrome (Orphanet:2461)
Marinesco-Sjögren syndrome (Orphanet:559)
Mesomelic dwarfism - cleft palate - camptodactyly (Orphanet:2631)
Mesomelic dysplasia, Savarirayan type (Orphanet:85170)
Metaphyseal acroscyphodysplasia (Orphanet:1240)
Metaphyseal chondrodysplasia, Schmid type (Orphanet:174)
Metaphyseal chondrodysplasia, Spahr type (Orphanet:2501)
Metaphyseal dysostosis - intellectual deficit - conductive deafness (Orphanet:2502)
Micrencephaly - corpus callosum agenesis - abnormal genitalia (Orphanet:2508)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Microcephalic primordial dwarfism, Dauber type (Orphanet:319675)
Microcephaly - cervical spine fusion anomalies (Orphanet:2522)
Microspherophakia - metaphyseal dysplasia (Orphanet:2551)
Mietens syndrome (Orphanet:2557)
Mosaic trisomy 9 (Orphanet:99776)
Mucolipidosis type 3 (Orphanet:577)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 3 (Orphanet:581)
Mucopolysaccharidosis type 4 (Orphanet:582)
Mucopolysaccharidosis type 6 (Orphanet:583)
Mucopolysaccharidosis type 7 (Orphanet:584)
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 4 (Orphanet:93307)
Multiple epiphyseal dysplasia type 5 (Orphanet:93311)
Multiple non-ossifying fibromatosis (Orphanet:2029)
Neurogenic arthrogryposis multiplex congenita (Orphanet:1143)
Non-rhizomelic chondrodysplasia punctata (Orphanet:176)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
Occipital horn syndrome (Orphanet:198)
Oculocerebral hypopigmentation syndrome, Preus type (Orphanet:2720)
Oculocerebrocutaneous syndrome (Orphanet:1647)
Oculocerebrorenal syndrome (Orphanet:534)
Okamoto syndrome (Orphanet:2729)
Osteochondrodysplatic nanism - deafness - retinitis pigmentosa (Orphanet:2653)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
Osteogenesis imperfecta (Orphanet:666)
Otopalatodigital syndrome (Orphanet:669)
Pelvic dysplasia - arthrogryposis of lower limbs (Orphanet:2840)
Pelvis-shoulder dysplasia (Orphanet:2839)
Pentasomy X (Orphanet:11)
Pfeiffer syndrome (Orphanet:710)
Prader-Willi syndrome (Orphanet:739)
Progressive pseudorheumatoid arthropathy of childhood (Orphanet:1159)
Prolidase deficiency (Orphanet:742)
Proteus syndrome (Orphanet:744)
Prune belly syndrome (Orphanet:2970)
Pseudoachondroplasia (Orphanet:750)
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency (Orphanet:88618)
Radio-ulnar synostosis - amegakaryocytic thrombocytopenia (Orphanet:71289)
Rhizomelic dysplasia, Patterson-Lowry type (Orphanet:2831)
Rhizomelic syndrome, Urbach type (Orphanet:3098)
Richieri Costa-Pereira syndrome (Orphanet:3102)
Rothmund-Thomson syndrome (Orphanet:2909)
Rubinstein-Taybi syndrome (Orphanet:783)
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY (OMIM:181405)
SHORT syndrome (Orphanet:3163)
SPONASTRIME dysplasia (Orphanet:93357)
STEVENSON-CAREY SYNDROME (OMIM:611961)
Satoyoshi syndrome (Orphanet:3130)
Say-Barber-Miller syndrome (Orphanet:3132)
Scheie syndrome (Orphanet:93474)
Schimke immuno-osseous dysplasia (Orphanet:1830)
Schwartz-Jampel syndrome (Orphanet:800)
Seckel syndrome (Orphanet:808)
Senior-Loken syndrome 8 (OMIM:616307)
Sheldon-Hall syndrome (Orphanet:1147)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Skeletal dysplasia - epilepsy - short stature (Orphanet:1858)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Sotos syndrome (Orphanet:821)
Splenogonadal fusion - limb defects - micrognathia (Orphanet:2063)
Spondyloepimetaphyseal dysplasia congenita, Strudwick type (Orphanet:93346)
Spondyloepimetaphyseal dysplasia with joint laxity (Orphanet:93359)
Spondyloepimetaphyseal dysplasia with multiple dislocations (Orphanet:93360)
Spondyloepimetaphyseal dysplasia, Irapa type (Orphanet:93351)
Spondyloepimetaphyseal dysplasia, Missouri type (Orphanet:93356)
Spondyloepimetaphyseal dysplasia, Shohat type (Orphanet:93352)
Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia (Orphanet:253)
Spondyloepiphyseal dysplasia congenita (Orphanet:94068)
Spondyloepiphyseal dysplasia tarda (Orphanet:93284)
Spondylometaphyseal dysplasia (Orphanet:254)
Spondylometaphyseal dysplasia - cone-rod dystrophy (Orphanet:85167)
Spondylometaphyseal dysplasia, 'corner fracture' type (Orphanet:93315)
Spondylometaphyseal dysplasia, A4 type (Orphanet:168555)
Spondylometaphyseal dysplasia, Kozlowski type (Orphanet:93314)
Steinert myotonic dystrophy (Orphanet:273)
Stickler syndrome (Orphanet:828)
THREE M SYNDROME 3 (OMIM:614205)
Tetrasomy X (Orphanet:9)
Thanatophoric dysplasia (Orphanet:2655)
Thrombocytopenia - absent radius (Orphanet:3320)
Trichodermodysplasia - dental alterations (Orphanet:3353)
Trichorhinophalangeal syndrome type 1 and 3 (Orphanet:77258)
Trismus - pseudocamptodactyly (Orphanet:3377)
Trisomy 18 (Orphanet:3380)
Trisomy 20p (Orphanet:261318)
Trisomy X (Orphanet:3375)
Ulna metaphyseal dysplasia syndrome (Orphanet:1837)
Upington disease (Orphanet:3408)
VACTERL with hydrocephalus (Orphanet:3412)
Weaver-Williams syndrome (Orphanet:3448)
Weismann-Netter syndrome (Orphanet:3344)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)
Wolcott-Rallison syndrome (Orphanet:1667)
Wolf-Hirschhorn syndrome (Orphanet:280)
Wrinkly skin syndrome (Orphanet:2834)
X-linked dominant chondrodysplasia punctata (Orphanet:35173)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)
Yunis-Varon syndrome (Orphanet:3472)
Zunich-Kaye syndrome (Orphanet:3474)
[DEL] ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1 (OMIM:208085)