Additional Disease Briefs

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growth delay due to insulin-like growth factor I resistance

Also known as: IGF-1 resistance, IGF-I resistance, IGF1RES, Somatomedin end-organ insensitivity to, Somatomedin, end-organ insensitivity to, Somatomedin-C, resistance to, Somatomedin-c resistance to, growth delay due to insulin-like growth factor I resistance, insulin-like Growth Factor I, resistance to, due to increased binding Protein, insulin-like growth factor 1 resistance to, insulin-like growth factor I, resistance to, resistance to IGF-1


growth delay due to insulin-like growth factor type 1 deficiency

Also known as: IGF-1 deficiency, IGF1 deficiency, growth delay-deafness- intellectual disability syndrome, growth retardation with deafness and mental retardation due to IGF1 deficiency, growth retardation with sensorineural deafness and intellectual disability, growth retardation with sensorineural deafness and mental retardation, insulin-like growth Factor 1 deficiency, insulin-like growth factor I deficiency, primary insulin-like growth factor deficiency





growth hormone-producing pituitary gland adenoma

Also known as: GH cell adenoma, Somatotrophinoma, growth hormone producing adenoma of pituitary, growth hormone producing adenoma of pituitary gland, growth hormone producing adenoma of the pituitary, growth hormone producing adenoma of the pituitary gland, growth hormone producing pituitary adenoma, growth hormone producing pituitary gland adenoma, growth hormone secreting adenoma of pituitary, growth hormone secreting adenoma of pituitary gland, growth hormone secreting adenoma of the pituitary, growth hormone secreting adenoma of the pituitary gland, growth hormone secreting pituitary adenoma, growth hormone secreting pituitary gland adenoma, growth hormone-producing adenoma, growth hormone-producing pituitary gland adenoma, somatotrope adenoma, somatotroph adenoma, somatotropic adenoma




Grubben-de Cock-Borghgraef syndrome

Also known as: Grubben de Cock Borghgraef syndrome, developmental delay - hypotonia - extremities hypertrophy, developmental delay-hypotonia-extremities hypertrophy syndrome, growth retardation, small and puffy hands and feet, and eczema, severe growth retardation, developmental delay with hypotonia, hypotrophy of the distal extremities, dental anomalies, and eczematous skin


GTP cyclohydrolase I deficiency with hyperphenylalaninemia

Also known as: GTP cyclohydrolase 1 deficiency, GTP cyclohydrolase I deficiency, GTPCH deficiency, HPABH4B, hyperphenylalaninemia due to GTP cyclohydrolase deficiency, hyperphenylalaninemia, BH4-deficient, B, hyperphenylalaninemia, Bh4-deficient, type B, hyperphenylalaninemia, tetrahydrobiopterin-deficient, due to GTP cyclohydrolase 1 deficiency