tietz syndrome

Preferred Label : tietz syndrome;

CISMeF synonym : hypopigmentation/deafness of tietz;

MeSH synonym : albinism-deafness of tietz; tietz albinism-deafness syndrome; albinism and complete nerve deafness; Hypopigmentation-deafness of Tietz;

Details

Origin ID

C536919;

UMLS CUI

C0391816;

Automatic exact mappings (from CISMeF team)
- Costochondritis [ICD-11 More detail]
- Musculoskeletal Chest Pain due to Costochondral Junction Syndrome [NCIt concept]
- musculoskeletal disease other [ICPC-2 Rubric]
Currated CISMeF NLP mapping
- Albinism-deafness syndrome of Tietz (disorder) [SNOMED CT concept]
- Chondrocostal junction syndrome [Tietze] [ICD-10 Sub-category (who)]
- Tietz albinism-deafness syndrome [OMIM Phenotype]
- Tietz syndrome [DO Concept]
- Tietz syndrome [Disease (Nov.)]
- Tietz syndrome [ORDO Disease]
- Tietze syndrome [PASCAL descriptor]
- Tietze's disease [MedDRA LLT]
- Tietze's disease [ICD-9 code]
- Tietze's disease (disorder) [SNOMED CT concept]
- Tietze's syndrome [DO Concept]
- Tietze's syndrome [MedDRA LLT]
- tietze's disease [SNOMED Notion]
Has phenotype(s) (HPO)
- Bilateral congenital sensorineural deafness [HPO term]
MeSH term(s) associated for indexing
- albinism, oculocutaneous [MeSH Descriptor]
- deafness [MeSH Descriptor]
Ne pas confondre avec
- tietze's syndrome [MeSH Descriptor]
ORDO relation(s)
- Tietz syndrome [ORDO Disease]
Record concept(s)
- Tietz syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Albinism-deafness syndrome of Tietz (disorder) [SNOMED CT concept]
- Tietz albinism-deafness syndrome [OMIM Phenotype]
- Tietz syndrome [ORDO Disease]

Keyword's position in hierarchy(ies) :

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