splenogonadal fusion limb defects micrognatia

Preferred Label : splenogonadal fusion limb defects micrognatia;

MeSH synonym : splenogonadal fusion limb defects syndrome; splenogonadal fusion with limb defects and micrognathia; splenogonadal fusion limb defect syndrome;

Details

Origin ID

C537318;

UMLS CUI

C1866745;

Currated CISMeF NLP mapping
- Splenogonadal fusion with limb defects and micrognathia [OMIM Phenotype]
- Splenogonadal fusion, limb defect, micrognathia syndrome (disorder) [SNOMED CT concept]
- Splenogonadal fusion-limb defects-micrognathia syndrome [ORDO Disease]
MeSH term(s) associated for indexing
- craniofacial abnormalities [MeSH Descriptor]
- gonads [MeSH Descriptor]
- limb deformities, congenital [MeSH Descriptor]
- spleen [MeSH Descriptor]
Record concept(s)
- Splenogonadal fusion limb defects micrognatia [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Splenogonadal fusion with limb defects and micrognathia [OMIM Phenotype]
- Splenogonadal fusion, limb defect, micrognathia syndrome (disorder) [SNOMED CT concept]
- Splenogonadal fusion-limb defects-micrognathia syndrome [ORDO Disease]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients