Myoglobinuria, autosomal dominant

Preferred Label : Myoglobinuria, autosomal dominant;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal dominant type;

Prefixed ID : %160010;

Details

Origin ID

160010;

UMLS CUI

C1834567;

Currated CISMeF NLP mapping
- Autosomal dominant myoglobinuria [ICD-11 More detail]
- Autosomal dominant myoglobinuria [ORDO Disease]
- Autosomal dominant myoglobinuria (disorder) [SNOMED CT concept]
- myoglobinuria, autosomal dominant [MeSH concept]
- myoglobinuria, autosomal dominant [MeSH Supplementary Concept]
DO Cross reference
- myoglobinuria [DO Concept]
HPO term(s)
- Acute kidney injury [HPO term]
- Autosomal dominant inheritance [HPO term]
- Elevated circulating creatine kinase concentration [HPO term]
- Muscle weakness [HPO term]
- Myalgia [HPO term]
- Myoglobinuria [HPO term]
ORDO concept(s)
- Autosomal dominant myoglobinuria [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant myoglobinuria [ORDO Disease]
- Autosomal dominant myoglobinuria [ICD-11 More detail]
- Autosomal dominant myoglobinuria (disorder) [SNOMED CT concept]
- myoglobinuria, autosomal dominant [MeSH Supplementary Concept]
- myoglobinuria, autosomal dominant [MeSH concept]

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