gerodermia osteodysplastica

Preferred Label : gerodermia osteodysplastica;

MeSH synonym : geroderma osteodysplastica hereditaria; walt disney dwarfism; geroderma osteodysplastica; geroderma osteodysplasticum;

Details

Origin ID

C537799;

UMLS CUI

C0432255;

Automatic exact mappings (from CISMeF team)
- golgin, RAB6 interacting [ORDO Gene]
- golgin, RAB6 interacting [HGNC gene]
CISMeF manual mappings
- Geroderma osteodysplastica [ORDO Disease]
Currated CISMeF NLP mapping
- Geroderma osteodysplastica (disorder) [SNOMED CT concept]
- Geroderma osteodysplasticum [ICD-11 More detail]
- Geroderma osteodysplasticum [OMIM Phenotype]
- Osteodysplastic gerodermia [PASCAL descriptor]
- geroderma osteodysplasticum [DO Concept]
- gerodermia osteodysplastica [Disease (Nov.)]
DO Cross reference
- geroderma osteodysplasticum [DO Concept]
MeSH term(s) associated for indexing
- bone diseases [MeSH Descriptor]
- dwarfism [MeSH Descriptor]
- skin diseases, genetic [MeSH Descriptor]
ORDO relation(s)
- Geroderma osteodysplastica [ORDO Disease]
Record concept(s)
- Gerodermia osteodysplastica [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Geroderma osteodysplastica [ORDO Disease]
- Geroderma osteodysplastica (disorder) [SNOMED CT concept]
- Geroderma osteodysplasticum [OMIM Phenotype]
- Geroderma osteodysplasticum [ICD-11 More detail]
- Osteodysplastic gerodermia [PASCAL descriptor]
- geroderma osteodysplasticum [DO Concept]
- gerodermia osteodysplastica [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

Main resources

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