Carbohydrate metabolism
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Lipid/glycolipid metabolism
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Nucleotide metabolism
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Amino acid metabolism
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Glycan/glycoprotein metabolism
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Cofactor/vitamin metabolism
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Replication and repair
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Signal transduction
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Cellular process
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Immune system
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Endocrine system
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nt06310 CRH-ACTH-cortisol signaling
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nt06322 TRH-TSH-TH signaling
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nt06323 KISS1-GnRH-LH/FSH-E2 signaling
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nt06324 GHRH-GH-IGF signaling
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nt06318 CaSR-PTH signaling
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nt06316 Renin-angiotensin-aldosterone signaling
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nt06325 Hormone/cytokine signaling
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H00250 Congenital nongoitrous hypothyroidism (CHNG)
H00408 Type 1 diabetes mellitus
H00410 Maturity onset diabetes of the young (MODY)
H01228 Insulin-resistant diabetes mellitus with acanthosis nigricans
H00719 Leprechaunism
H00942 Rabson-Mendenhall syndrome
H01267 Familial hyperinsulinemic hypoglycemia
H01388 Hyperprolactinemia
H01294 Nephrogenic syndrome of inappropriate antidiuresis
H00255 Hypogonadotropic hypogonadism
H00253 Neurohypophyseal diabetes insipidus
H02059 Leptin deficiency
H02060 Leptin receptor deficiency
H01193 Familial tumoral calcinosis
H00967 Adiponectin deficiency
H00214 Hypophosphatemic rickets
H00240 Gitelman syndrome
H01371 Hypercalcemia infantile
H01293 Narcolepsy
H00809 Familial epilepsy temporal lobe (ETL)
H00265 Hereditary sensory and autonomic neuropathy
H02674 Atrial standstill
H00731 Atrial fibrillation
H00801 Familial thoracic aortic aneurysm and dissection
H00759 Waardenburg syndrome
H01198 Fanconi renotubular syndrome
H00243 Hyperkalemic distal renal tubular acidosis (RTA type 4)
H00888 Nephrolithiasis/osteoporosis, hypophosphatemic
H00512 Permanent neonatal diabetes mellitus
H00910 Hirschsprung disease
H02185 Spondylometaphyseal dysplasia
H02543 Acromesomelic dysplasia
H01884 Auriculocondylar syndrome
H02679 Miura-type epiphyseal chondrodysplasia
H02126 Mandibulofacial dysostosis with alopecia
H00823 ABCD syndrome
H02681 Short stature with nonspecific skeletal abnormalities
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nt06320 APOB-LDLR signaling
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