Hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation 1

Preferred Label : Hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation 1;

Symbol : HUMOP1;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Luft syndrome; Hypermetabolism due to defect in mitochondria;

Inheritance : ? Autosomal recessive;

Prefixed ID : 238800;

Details

Origin ID

238800;

UMLS CUI

C1855926;

Currated CISMeF NLP mapping
- hypermetabolism due to defect in mitochondria [MeSH concept]
- hypermetabolism due to defect in mitochondria [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of metabolism/homeostasis [HPO term]
- Autosomal recessive inheritance [HPO term]
Not associated HPO term(s)
- Abnormality of thyroid physiology [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- hypermetabolism due to defect in mitochondria [MeSH Supplementary Concept]
- hypermetabolism due to defect in mitochondria [MeSH concept]

Keyword's position in hierarchy(ies) :

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