Trichorrhexis nodosa syndrome

Preferred Label : Trichorrhexis nodosa syndrome;

Obsolete resource : true;

Moved to : 234050;

Alternative titles and symbols : Pollitt syndrome; Trichothiodystrophy-neurocutaneous syndrome;

Inheritance : Autosomal recessive;

Prefixed ID : 275550;

Détails

Origin ID

275550;

UMLS CUI

C1313961;

Currated CISMeF NLP mapping
- Pollitt syndrome [ORDO Disease]
- Trichorrhexis nodosa [ICD-10 Sub-category (who)]
- Trichorrhexis nodosa [ICD-10 Sub-category]
- Trichorrhexis nodosa syndrome [ICD-11 More detail]
- Trichorrhexis nodosa syndrome [MeSH concept]
- trichorrhexis nodosa syndrome [MeSH Supplementary Concept]
HPO term(s)
- Ichthyosis [HPO term]
- Receding chin [HPO term]
ORDO concept(s)
- Pollitt syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Pollitt syndrome [ORDO Disease]
- Trichorrhexis nodosa syndrome [MeSH concept]
- Trichothiodystrophy 4, Nonphotosensitive [NCIt concept]
- trichorrhexis nodosa syndrome [MeSH Supplementary Concept]
Validated automatic mappings to BTNT
- Clastothrix (disorder) [SNOMED CT concept]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients