Hydronephrosis, congenital, with cleft palate, characteristic facies, hypotonia, and mental retardation

Preferred Label : Hydronephrosis, congenital, with cleft palate, characteristic facies, hypotonia, and mental retardation;

Obsolete resource : true;

Moved to : 616580;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Okamoto syndrome;

Prefixed ID : 604916;

Details

Origin ID

604916;

UMLS CUI

C1858043;

Automatic exact mappings (from CISMeF team)
- hydronephrosis, congenital, with cleft palate, characteristic facies, hypotonia, and mental retardation [MeSH concept]
Currated CISMeF NLP mapping
- Okamoto syndrome [ORDO Disease]
- Okamoto syndrome (disorder) [SNOMED CT concept]
- hydronephrosis, congenital, with cleft palate, characteristic facies, hypotonia, and mental retardation [MeSH Supplementary Concept]
ORDO concept(s)
- Okamoto syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Okamoto syndrome [ORDO Disease]
- Okamoto syndrome (disorder) [SNOMED CT concept]
- hydronephrosis, congenital, with cleft palate, characteristic facies, hypotonia, and mental retardation [MeSH Supplementary Concept]
- hydronephrosis, congenital, with cleft palate, characteristic facies, hypotonia, and mental retardation [MeSH concept]

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