Hip dysplasia
Symptom Information:
Symptom ID: | HPO:0001385 | ||||||||||||||||||||||||||
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 lower limb joint(HPO:0100491) Abnormality of the hip bone(HPO:0003272) Hip dysplasia(HPO:0001385) Abnormal appendicular skeleton morphology(HPO:0011844) Abnormality of pelvic girdle bone morphology(HPO:0002644) Abnormality of the hip bone(HPO:0003272) Hip dysplasia(HPO:0001385) 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) 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) |
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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) |