Hyperphosphatemia, polyuria, and seizures

Preferred Label : Hyperphosphatemia, polyuria, and seizures;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal recessive;

Prefixed ID : 239350;

Details

Origin ID

239350;

UMLS CUI

C1855922;

Currated CISMeF NLP mapping
- hyperphosphatemia, polyuria, and seizures [MeSH concept]
- hyperphosphatemia, polyuria, and seizures [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of the voice [HPO term]
- Autosomal recessive inheritance [HPO term]
- Diarrhea [HPO term]
- Fever [HPO term]
- High-pitched cry [HPO term]
- Hyperphosphatemia [HPO term]
- Irritability [HPO term]
- Polyuria [HPO term]
- Seizure [HPO term]
- Tetany [HPO term]
- Vomiting [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- hyperphosphatemia, polyuria, and seizures [MeSH Supplementary Concept]
- hyperphosphatemia, polyuria, and seizures [MeSH concept]

Keyword's position in hierarchy(ies) :

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