respiratory paralysis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Inability to move the muscles of respiration. (Human Phenotype Ontology, HP_0002203)
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3 genes associated with the respiratory paralysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALAD aminolevulinate dehydratase
CPOX coproporphyrinogen oxidase
HMBS hydroxymethylbilane synthase