Introduction
Pocket Metab
Impressum
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Diseases
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Symptoms
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Lab Parameters
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Authors
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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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HARTNUP DISEASE
HAWKINSINURIA
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1
HEPATOERYTHROPOIETIC PROPHYRIA (HEP)
HEREDITARY COPROPORPHYRIA (HCP)
HISTIDINEMIA
HISTIDINURIA
HOMOCARNOSINOSIS
HOMOCYSTINURIA DUE TO DEFECT OF N(5,10)-METHYLENE THF DEFICIENCY
HOMOCYSTINURIA, CblE TYPE OF
HOMOCYSTINURIA, CYSTATHIONINE BETA-SYNTHASE DEFICIENCY
HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA DUE TO DEFECT IN COBALAMIN METABOLISM, cblG COMPLEMENTATION TYPE
HUMAN GROWTH HORMONE DEFICIENCY
HYDROPS FETALIS, NON IMMUNE
HYDROXYKYNURENINURIA
HYDROXYLYSINURIA
HYDROXYPROLINEMIA
HYPER BETA-ALANINEMIA
HYPER-IgD SYNDROME
HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, TYPE B
HYPERCHOLESTEROLEMIA, FAMILIAL
HYPERCYSTINURIA
HYPERDIBASIC AMINOACIDURIA I
HYPEREKPLEXIA
HYPERGLYCINEMIA, NON-KETOTIC
HYPERINSULINISM-HYPERAMMONEMIA SYNDROME
HYPERKYNURENINURIA
HYPERLYSINEMIA I, FAMILIAL
HYPERLYSINEMIA II OR SACCHAROPINURIA
HYPERLYSINURIA
HYPERORNITHINEMIA WITH GYRATE ATROPHY (HOGA)
HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA [HHH-SYNDROME]
HYPERPHENYLALANIEMIA DUE TO GUANOSINE TRIPHOSPHATE CYCLOHYDROLASE DEFICIENCY
HYPERPHENYLALANINEMIA DUE TO 6-PYRUVOYLTETRAHYDROPTERIN SYNTHASE DEFICIENCY (PTPS)
HYPERPHENYLALANINEMIA DUE TO DHPR-DEFICIENCY
HYPERPHENYLALANINEMIA DUE TO PTERIN-4a-CARBINOLAMINE DEHYDRATASE
HYPERPHOSPHATASIA
HYPERPIPECOLATEMIA
HYPERPROLINEMIA, TYPE I
HYPERPROLINEMIA, TYPE II
HYPERTRIGLYCERIDEMIA
HYPERVALINEMIA
HYPERZINCAEMIA AND HYPERCALPROTECTINAEMIA
HYPOADRENOCORTICISM, FAMILIAL
HYPOGLYCEMIA, FAMILIAL NEONATAL
HYPOMAGNESEMIA WITH SECONDARY HYPOCALCEMIA
HYPOPHOSPHATASIA
HYPOTHYROIDISM, CONGENITAL
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