Disease Browser
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Parent Node: Deafness (D003638) | Parent Node: Growth Disorders (D006130) | Parent Node: Hip Dislocation, Congenital (D006618) | ..Starting node ..Coxoauricular Syndrome (C565148)
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Sister Nodes: | ..Camptodactyly syndrome Guadalajara type 2 (C537971)
| ..Carnevale syndrome (C535586)
| ..CODAS syndrome (C536434)
| ..Coxoauricular Syndrome (C565148)
| ..DEVELOPMENTAL DYSPLASIA OF THE HIP 1 (OMIM:142700)
| ..Dislocation of Hip, Congenital, with Hyperextensibility of Fingers and Facial Dysmorphism (C563315)
| ..Dwarfism tall vertebrae (C535725)
| ..Dwarfism, Proportionate, with Hip Dislocation (C565614)
| ..Hip Dysplasia, Beukes Type (C564185)
| ..Ho Kaufman Mcalister syndrome (C538325)
| ..Keratoconus And Congenital Hip Dysplasia (C565456)
| ..Neurologic Disease, Infantile Multisystem, with Osseous Fragility (C564954)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 2798 |
Name: | Coxoauricular Syndrome |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D003638|MESH:D006130|MESH:D006618 |
TreeNumbers: | C05.660.449/C565148 |C09.218.458.341.186/C565148 |C10.597.751.418.341.186/C565148 |C16.131.621.449/C565148 |C23.550.393/C565148 |C23.888.592.763.393.341.186/C565148 |
Synonyms: | |
Slim Mappings: | Congenital abnormality|Ear-nose-throat disease|Musculoskeletal disease|Nervous system disease|Pathology (process)|Signs and symptoms |
Reference: |
MedGen: C565148
MeSH: C565148
OMIM: 122780;
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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