Pagod syndrome

Preferred Label : Pagod syndrome;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Agonadism with multiple internal malformations;

Prefixed ID : 202660;

Details

Origin ID

202660;

UMLS CUI

C1859967;

Automatic exact mappings (from CISMeF team)
- Pulmonary hypoplasia, agonadism, dextrocardia, diaphragmatic hernia syndrome (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Agonadism - dextrocardia - diaphragmatic hernia [ICD-11 More detail]
- Kennerknecht Sorgo Oberhoffer syndrome [MeSH concept]
- PAGOD syndrome [ORDO Disease]
- kennerknecht sorgo oberhoffer syndrome [MeSH Supplementary Concept]
ORDO concept(s)
- PAGOD syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Agonadism - dextrocardia - diaphragmatic hernia [ICD-11 More detail]
- Kennerknecht Sorgo Oberhoffer syndrome [MeSH concept]
- PAGOD syndrome [ORDO Disease]
- Pulmonary hypoplasia, agonadism, dextrocardia, diaphragmatic hernia syndrome (disorder) [SNOMED CT concept]
- kennerknecht sorgo oberhoffer syndrome [MeSH Supplementary Concept]

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