FLOTCH syndrome

Preferred Label : FLOTCH syndrome;

MeSH note : Familial occurrence of total Leukonychia, Trichilemmal cysts and Ciliary dystrophy with dominant autosomal Heredity;

MeSH synonym : friedel heid grosshans syndrome;

Details

Origin ID

C537065;

UMLS CUI

C2931411;

Automatic exact mappings (from CISMeF team)
- Leukonychia totalis, trichilemmal cysts, ciliary dystrophy syndrome (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- FLOTCH syndrome [ORDO Disease]
MeSH term(s) associated for indexing
- blepharitis [MeSH Descriptor]
- epidermal cyst [MeSH Descriptor]
- hair diseases [MeSH Descriptor]
- nail diseases [MeSH Descriptor]
- pigmentation disorders [MeSH Descriptor]
- retinal diseases [MeSH Descriptor]
ORDO relation(s)
- FLOTCH syndrome [ORDO Disease]
Record concept(s)
- FLOTCH syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- FLOTCH syndrome [ORDO Disease]
- Leukonychia totalis, trichilemmal cysts, ciliary dystrophy syndrome (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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