Congenital hip dislocation
Symptom Information:
Symptom ID: | HPO:0001374 | ||||||||||||
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 appendicular skeleton morphology(HPO:0011844) Abnormality of pelvic girdle bone morphology(HPO:0002644) Abnormality of the hip bone(HPO:0003272) Abnormality of the hip joint(HPO:0001384) Hip dislocation(HPO:0002827) Congenital hip dislocation(HPO:0001374) 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) Abnormality of the hip joint(HPO:0001384) Hip dislocation(HPO:0002827) Congenital hip dislocation(HPO:0001374) Abnormal joint morphology(HPO:0001367) Abnormality of lower limb joint(HPO:0100491) Abnormality of the hip bone(HPO:0003272) Abnormality of the hip joint(HPO:0001384) Hip dislocation(HPO:0002827) Congenital hip dislocation(HPO:0001374) Joint dislocation(HPO:0001373) Hip dislocation(HPO:0002827) Congenital hip dislocation(HPO:0001374) MedDRA: |
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Database Frequency: | 51 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
ALDH18A1-related De Barsy syndrome | (Orphanet:35664) |
AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM | (OMIM:104350) |
ARTHROGRYPOSIS, DISTAL, TYPE 1A | (OMIM:108120) |
AXENFELD-RIEGER SYNDROME, TYPE 2 | (OMIM:601499) |
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) |
BOR syndrome | (Orphanet:107) |
BRITTLE CORNEA SYNDROME 1 | (OMIM:229200) |
Blepharophimosis-intellectual deficit syndrome due to UBE3B deficiency | (Orphanet:329255) |
Brittle cornea syndrome | (Orphanet:90354) |
CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURALHEARING LOSS, AND SKELETAL DYSPLASIA | (OMIM:616007) |
CHILD syndrome | (Orphanet:139) |
CODAS syndrome | (Orphanet:1458) |
Central core disease | (Orphanet:597) |
Cerebro-costo-mandibular syndrome | (Orphanet:1393) |
Cloacal exstrophy | (Orphanet:93929) |
Congenital anonychia | (Orphanet:79143) |
Congenital fiber-type disproportion myopathy | (Orphanet:2020) |
DEVELOPMENTAL DYSPLASIA OF THE HIP 1 | (OMIM:142700) |
De Barsy syndrome | (Orphanet:2962) |
Digitotalar dysmorphism | (Orphanet:1146) |
Dislocation of the hip - dysmorphism | (Orphanet:2412) |
Ehlers-Danlos syndrome type 11 | (Orphanet:2295) |
Emanuel syndrome | (Orphanet:96170) |
Endosteal sclerosis - cerebellar hypoplasia | (Orphanet:85186) |
Exstrophy-epispadias complex | (Orphanet:322) |
Focal dermal hypoplasia | (Orphanet:2092) |
Fuhrmann syndrome | (Orphanet:2854) |
Genitopatellar syndrome | (Orphanet:85201) |
Gordon syndrome | (Orphanet:376) |
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6 | (OMIM:614450) |
Hurler-Scheie syndrome | (Orphanet:93476) |
KABUKI SYNDROME 1 | (OMIM:147920) |
Kabuki syndrome | (Orphanet:2322) |
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION | (OMIM:255310) |
McKusick-Kaufman syndrome | (Orphanet:2473) |
Moderate multiminicore disease with hand involvement | (Orphanet:178145) |
Oculocerebrocutaneous syndrome | (Orphanet:1647) |
Otopalatodigital syndrome | (Orphanet:669) |
Otopalatodigital syndrome type 2 | (Orphanet:90652) |
Pelvis-shoulder dysplasia | (Orphanet:2839) |
Postaxial acrofacial dysostosis | (Orphanet:246) |
Prune belly syndrome | (Orphanet:2970) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Simpson-Golabi-Behmel syndrome type 2 | (Orphanet:79022) |
Spondyloepimetaphyseal dysplasia with multiple dislocations | (Orphanet:93360) |
Tetrasomy 12p | (Orphanet:884) |
URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME | (OMIM:300280) |
Wrinkly skin syndrome | (Orphanet:2834) |