" /> Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency - CISMeF





Preferred Label : Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal recessive;

Prefixed ID : #613752;

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03/05/2025


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