Hearing Loss Disease Portal


 
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Parent Node:
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Musculoskeletal Abnormalities (D009139)
..Starting node
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Hip Dislocation, Congenital (D006618)

       Child Nodes:
........expandCamptodactyly syndrome Guadalajara type 2 (C537971)
........expandCarnevale syndrome (C535586)
........expandCODAS syndrome (C536434)
........expandCoxoauricular Syndrome (C565148)
........expandDEVELOPMENTAL DYSPLASIA OF THE HIP 1 (OMIM:142700)
........expandDislocation of Hip, Congenital, with Hyperextensibility of Fingers and Facial Dysmorphism (C563315)
........expandDwarfism tall vertebrae (C535725)
........expandDwarfism, Proportionate, with Hip Dislocation (C565614)
........expandHip Dysplasia, Beukes Type (C564185)
........expandHo Kaufman Mcalister syndrome (C538325)
........expandKeratoconus And Congenital Hip Dysplasia (C565456)
........expandNeurologic Disease, Infantile Multisystem, with Osseous Fragility (C564954)



 Sister Nodes: 
..expandAbsent patella (C535568)
..expandACROPECTOROVERTEBRAL DYSPLASIA (OMIM:102510)
..expandArthrogryposis (D001176) Child55
..expandCampomelic Dysplasia (D055036) Child6
..expandCervical Rib Syndrome (D002573) Child1
..expandChondrodysplasia, Grebe type (C537915)
..expandCongenital absence of gluteal muscles (C535561)
..expandCongenital absence of the sternocleidomastoid muscle (C535977)
..expandCongenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi (C567863)
..expandCraniofacial Abnormalities (D019465) Child685
..expandFunnel Chest (D005660) Child4
..expandGastroschisis (D020139) Child1
..expandHajdu-Cheney Syndrome (D031845) Child1
..expandHip Dislocation, Congenital (D006618) Child12
..expandKlippel-Feil Syndrome (D007714) Child5
..expandLarsen syndrome, recessive type (C537874)
..expandLaryngomalacia (D055092) Child1
..expandLimb Deformities, Congenital (D017880) Child495
..expandPectus Carinatum (D066166)
..expandPseudoarthrogryposis (C566753)
..expandPterygium, Antecubital (C566738)
..expandSacrococcygeal dysgenesis association (C537225)
..expandSternal cleft (C537489)
..expandSynostosis (D013580) Child150
..expandTracheobronchomalacia (D055089) Child4
..expandVACTERL Association With Hydrocephalus (C564751)
..expandWidow's Peak Syndrome (C564040)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:5189
Name:Hip Dislocation, Congenital
Definition:Congenital dislocation of the hip generally includes subluxation of the femoral head, acetabular dysplasia, and complete dislocation of the femoral head from the true acetabulum. This condition occurs in approximately 1 in 1000 live births and is more common in females than in males.
Alternative IDs:
ParentIDs:MESH:D009139
TreeNumbers:C05.660.449 |C16.131.621.449
Synonyms:Congenital Dysplasia Of The Hip |Congenital Hip Dislocation |Congenital Hip Dislocations |Congenital Hip Displacement |Congenital Hip Displacements |Congenital Hip Dysplasia |Congenital Hip Dysplasias |Dislocation, Congenital Hip |Dislocation Of Hip, Congenital |
Slim Mappings:Congenital abnormality|Musculoskeletal disease
Reference: MedGen: D006618
MeSH: D006618
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants