Introduction
Pocket Metab
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Diseases
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Lab Parameters
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Ramedis
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BH4 Patient
Metabolic Information Centre (MIC) is designed to support the diagnosis of inborn errors of metabolism in a practical approach.
Together with our patient database RAMEDIS (www.ramedis.de) it is the basis of an expert system
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S-ADENOSYLHOMOCYSTEINE HYDROLASE DEFICIENCY
SALLA DISEASE
SARCOSINEMIA
SEGAWA SYNDROME
SENGERS SYNDROME
SEPIAPTERIN REDUCTASE DEFICIENCY
SEPSIS, NEONATAL [DD]
SERINE DEFIENCY SYNDROME - NEW DISEASE?
SHORT CHAIN ACYL-COA DEHYDROGENASE DEFICIENCY (SCAD)
SHORT-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY (SCHAD)
SHORT/BRANCHED-CHAIN ACYL-CoA DEHYDROGENASE DEFICIENCY
SIALIC ACID STORAGE DISEASE, INFANTILE TYPE
SIALIDOSIS TYPE I
SIALIDOSIS TYPE II
SMITH-LEMLI-OPITZ SYNDROME
SOTOS SYNDROME
SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY
SUCCINYL CoA: 3-KETOACID CoA TRANSFERASE DEFICIENCY
SUCRASE-ISOMALTASE DEFICIENCY
SULFITE OXIDASE DEFICIENCY
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