loading...| Preferred Name |
Otosclerosis |
|
| Synonyms |
Otosclerosis Localized Bone Dysplasia |
|
| Definitions |
A usually autosomal dominant inherited metabolic disorder affecting the bony labyrinth of the inner ear. Morphologically, it is characterized by the presence of sharply demarcated active (otospongiotic) and inactive (sclerotic) bony areas. It is one of the most common causes of conductive hearing loss. |
|
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C185242 |
|
| code |
C185242 |
|
| Concept_In_Subset | ||
| Contributing_Source |
Cellosaurus |
|
| DEFINITION |
A usually autosomal dominant inherited metabolic disorder affecting the bony labyrinth of the inner ear. Morphologically, it is characterized by the presence of sharply demarcated active (otospongiotic) and inactive (sclerotic) bony areas. It is one of the most common causes of conductive hearing loss. |
|
| FULL_SYN |
Otosclerosis Localized Bone Dysplasia |
|
| label |
Otosclerosis |
|
| Preferred_Name |
Otosclerosis |
|
| prefixIRI |
Thesaurus:C185242 |
|
| Semantic_Type |
Disease or Syndrome |
|
| UMLS_CUI |
C0029899 |
|
| subClassOf |