fibrochondrogenesis

Preferred Label : fibrochondrogenesis;

Origin ID

C562524;

UMLS CUI

C0265282;

Currated CISMeF NLP mapping
- Fibrochondrogenesis [PASCAL descriptor]
- Fibrochondrogenesis [ICD-11 More detail]
- Fibrochondrogenesis [OMIM phenotypic series]
- Fibrochondrogenesis [ORDO Disease]
- Fibrochondrogenesis (disorder) [SNOMED CT concept]
- fibrochondrogenesis [DO Concept]
- fibrochondrogenesis [Disease (Nov.)]
- fibrochondrogenesis [SNOMED Notion]
DO Cross reference
- fibrochondrogenesis [DO Concept]
MeSH term(s) associated for indexing
- abnormalities, multiple [MeSH Descriptor]
- dwarfism [MeSH Descriptor]
- facies [MeSH Descriptor]
Record concept(s)
- fibrochondrogenesis [MeSH concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Fibrochondrogenesis [ORDO Disease]
- Fibrochondrogenesis [PASCAL descriptor]
- Fibrochondrogenesis [ICD-11 More detail]
- Fibrochondrogenesis (disorder) [SNOMED CT concept]
- fibrochondrogenesis [SNOMED Notion]
- fibrochondrogenesis [DO Concept]
- fibrochondrogenesis [Disease (Nov.)]
Validated automatic mappings to BTNT
- Fibrochondrogenesis 1 [OMIM Phenotype]