Iminoglycinuria (IG)

Iminoglycinuria(来自ICD-11)
别称:
Iminoglycinuria, Digenic
Ig
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Basic Information
Medical Symptom
Gene & Mutation
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References Literature
Iminoglycinuria, also known as ig, is related to hyperglycinuria and aminoaciduria. An important gene associated with Iminoglycinuria is SLC36A2 (Solute Carrier Family 36 Member 2), and among its related pathways/superpathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Nuclear receptors meta-pathway. Affiliated tissues include kidney and eye, and related phenotypes are prolinuria and hydroxyprolinuria
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MALACARDS
AR
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38
196
10

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