| Disease Browser
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Parent Node:
 inborn errors of metabolism (MONDO:0019052) |
..Starting node
.. inborn metal metabolism disorder ()
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Child Nodes:
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| ........acrodermatitis enteropathica () |
| ........atransferrinemia () |
| ........familial periodic paralysis () |
| ........familial primary hypomagnesemia () |
| ........hereditary hemochromatosis () |
| ........Menkes disease () |
| ........pseudohypoparathyroidism () |
| ........sulfite oxidase deficiency due to molybdenum cofactor deficiency () |
| ........Wilson disease () |
Sister Nodes: |
..abdominal obesity-metabolic syndrome 3 ()
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..alcohol sensitivity, acute ()  L: 00081;
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..Alstrom syndrome ()
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..apolipoprotein c-III deficiency ()
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..AREDYLD syndrome ()
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..aromatase excess syndrome ()
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..autosomal dominant hypocalcemia ()
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..autosomal recessive infantile hypercalcemia ()
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..Bloom syndrome ()
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..Cockayne syndrome ()
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..diabetes mellitus, noninsulin-dependent, 1 ()
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..diabetes mellitus, noninsulin-dependent, 3 ()
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..diabetes mellitus, noninsulin-dependent, 4 ()
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..diabetes mellitus, noninsulin-dependent, 5 ()
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..diabetic ketoacidosis ()
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..disorder of lysosomal-related organelles ()
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..disorder of metabolite absorption and transport ()
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..Donohue syndrome ()
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..familial calcium pyrophosphate deposition ()
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..familial hyperinsulinism ()
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..familial hypocalciuric hypercalcemia ()
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..familial intrahepatic cholestasis ()
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..familial tumoral calcinosis ()
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..ferro-cerebro-cutaneous syndrome ()
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..gluthathione peroxidase deficiency ()
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..H syndrome ()
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..hereditary amyloidosis ()
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..hereditary chronic pancreatitis ()
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..hereditary thrombophilia due to congenital protein C deficiency ()
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..hypophosphatasia ()
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..immunodeficiency-centromeric instability-facial anomalies syndrome ()
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..immunoglobulin-mediated membranoproliferative glomerulonephritis ()
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..inborn disorder of amino acid and other organic acid metabolism ()
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..inborn disorder of porphyrin metabolism ()
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..inborn metal metabolism disorder ()
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..inborn vitamin metabolic disorder ()
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..inherited lipid metabolism disorder ()
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..insulin-resistance syndrome type A ()
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..juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome ()
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..lysosomal storage disease ()
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..mannose-binding lectin deficiency ()
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..metabolic syndrome X ()
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..microcephalic primordial dwarfism-insulin resistance syndrome ()
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..neonatal diabetes mellitus with congenital hypothyroidism ()
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..NIDDM2 ()
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..Nijmegen breakage syndrome ()
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..Nijmegen breakage syndrome-like disorder ()
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..nucleoside diphosphate-linked moiety X Motif 15 deficiency ()
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..permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome ()
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..peroxisomal disease ()
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..photosensitive trichothiodystrophy ()
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..plasma protein metabolism disease ()
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..polyendocrine-polyneuropathy syndrome ()
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..polysyndactyly ()
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..primary microcephaly-epilepsy-permanent neonatal diabetes syndrome ()
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..primary microcephaly-mild intellectual disability-young-onset diabetes syndrome ()
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..proximal renal tubular acidosis ()
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..Rabson-Mendenhall syndrome ()
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..recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome ()
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..renal tubular acidosis 3 ()
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..renal tubular acidosis, distal, autosomal recessive ()
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..severe combined immunodeficiency due to DCLRE1C deficiency ()
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..thiopurine S-methyltransferase deficiency ()
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..UV-sensitive syndrome ()
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..Waldenstrom macroglobulinemia ()
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..Wolcott-Rallison syndrome ()
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MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
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