myoglobinuria, acute recurrent, autosomal recessive

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Myoglobinuria, acute recurrent, autosomal recessive
LPIN1 Causal
18817903
ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with myoglobinuria, acute recurrent, autosomal recessive.
3 View disease cluster →
Genetic recurrent myoglobinuria 1 shared geneLPIN1 Related via 1 shared gene including LPIN1. Digestive system neoplasms 1 shared geneLPIN1 Related via 1 shared gene including LPIN1. Neoplasms 1 shared geneLPIN1 Related via 1 shared gene including LPIN1.