Congenital hip dislocation

Symptom Information:

Symptom ID: HPO:0001374
Synonyms:
Congenital dislocation of the hip [HPO:0001374]
Congenital dislocation of the hips [HPO:0001374]
Congenital hip anomaly [HPO:0001374]
Congenital hip dislocations [HPO:0001374]
Congenital dislocation of the hip [OMIM:Congenital dislocation of the hip]
Congenital dislocation of the hips [OMIM:Congenital dislocation of the hips]
Congenital hip anomaly [OMIM:Congenital hip anomaly]
Congenital hip dislocation [OMIM:Congenital hip dislocation]
Congenital hip dislocations [OMIM:Congenital hip dislocations]
Congenital dislocation of the hips (in 13%) [OMIM:Congenital dislocation of the hips (in 13%)]
Congenital hip anomalies [OMIM:Congenital hip anomalies]
Congenital hip dislocation (rare) [OMIM:Congenital hip dislocation (rare)]
Quality:
Cross references:
OMIM: "Congenital dislocation of the hip" [OMIM:Congenital dislocation of the hip]
OMIM: "Congenital dislocation of the hips" [OMIM:Congenital dislocation of the hips]
OMIM: "Congenital hip anomaly" [OMIM:Congenital hip anomaly]
OMIM: "Congenital hip dislocation" [OMIM:Congenital hip dislocation]
OMIM: "Congenital hip dislocations" [OMIM:Congenital hip dislocations]
OMIM: "Congenital dislocation of the hips (in 13%)" [OMIM:Congenital dislocation of the hips (in 13%)]
OMIM: "Congenital hip anomalies" [OMIM:Congenital hip anomalies]
OMIM: "Congenital hip dislocation (rare)" [OMIM:Congenital hip dislocation (rare)]
Is a (Direct Parents):
HPO         Hip 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)
                            Abnormality of the hip joint(HPO:0001384)
                               Hip dislocation(HPO:0002827)
                                  Congenital hip dislocation(HPO:0001374)
                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)
             Abnormal joint morphology(HPO:0001367)
                Joint dislocation(HPO:0001373)
                   Hip dislocation(HPO:0002827)
                      Congenital hip dislocation(HPO:0001374)
                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)
MedDRA:
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)