Vater-Like defects with pulmonary hypertension, laryngeal webs, and growth deficiency

Preferred Label : Vater-Like defects with pulmonary hypertension, laryngeal webs, and growth deficiency;

Origin ID

C564244;

UMLS CUI

C1842082;

CISMeF manual mappings
- Braddock syndrome (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Vater-like defects with pulmonary hypertension, laryngeal webs, and growth deficiency [OMIM Phenotype]
MeSH term(s) associated for indexing
- ear [MeSH Descriptor]
- growth disorders [MeSH Descriptor]
- heart defects, congenital [MeSH Descriptor]
- hypertension, pulmonary [MeSH Descriptor]
- larynx [MeSH Descriptor]
- spine [MeSH Descriptor]
Record concept(s)
- Vater-Like defects with pulmonary hypertension, laryngeal webs, and growth deficiency [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Braddock syndrome [ORDO Disease]
- Vater-like defects with pulmonary hypertension, laryngeal webs, and growth deficiency [OMIM Phenotype]