ONKI3 | Medical Subject Headings

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Dwarfism ∟ Laron Syndrome 6 coordinate concepts ∟ Achondroplasia \| ∟ Cockayne Syndrome \| ∟ Congenital Hypothyroidism \| ∟ Dwarfism, Pituitary \| ∟ Mulibrey Nanism \| ∟ Thanatophoric Dysplasia Medical Subject Headings (MeSH) ∟ Endocrine System Diseases ∟ Dwarfism ∟ Laron Syndrome 6 coordinate concepts ∟ Achondroplasia \| ∟ Cockayne Syndrome \| ∟ Congenital Hypothyroidism \| ∟ Dwarfism, Pituitary \| ∟ Mulibrey Nanism \| ∟ Thanatophoric Dysplasia Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Developmental ∟ Dwarfism ∟ Laron Syndrome 6 coordinate concepts ∟ Achondroplasia \| ∟ Cockayne Syndrome \| ∟ Congenital Hypothyroidism \| ∟ Dwarfism, Pituitary \| ∟ Mulibrey Nanism \| ∟ Thanatophoric Dysplasia X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Dwarfism ∟ Laron Syndrome Medical Subject Headings (MeSH) ∟ Endocrine System Diseases ∟ Dwarfism ∟ Laron Syndrome Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Developmental ∟ Dwarfism ∟ Laron Syndrome Dwarfism > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Dwarfism > Endocrine System Diseases > Medical Subject Headings (MeSH) Dwarfism > Bone Diseases, Developmental > Bone Diseases > Musculoskeletal Diseases > Medical Subject Headings (MeSH) X
History note:	Dwarfism (1976-2004) \| Growth Hormone (1976-2004) \| Receptors, Cell Surface (1976-2004) \| Receptors, Somatotropin (1991-2004)X
historyNote*:	2005 X
publicMeSHNote*:	2005 X
Scope note:	An autosomal recessive disorder characterized by short stature, defective GROWTH HORMONE RECEPTOR, and failure to generate INSULIN-LIKE GROWTH FACTOR I by GROWTH HORMONE. Laron syndrome is not a form of primary pituitary dwarfism (GROWTH HORMONE DEFICIENCY DWARFISM) but the result of mutation of the human GHR gene on chromosome 5. X
activeMeSHYear*:	2006 \| 2007X
dateCreated*:	2004-07-07X
dateEstablished*:	2005-01-01X
dateRevised*:	2005-06-30X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	lktX
Type:	Concept X
Coordinate terms:	Achondroplasia \| Cockayne Syndrome \| Congenital Hypothyroidism \| Dwarfism, Pituitary \| Mulibrey Nanism \| Thanatophoric Dysplasia X
URI:	X
Labels and equivalent concepts:	Laronin oireyhtymä (fi) Laronin syndrooma (fi, replaced) Larons syndrom (sv) GH-överkänslighet (sv, replaced) Severe GH Insensitivity (en, replaced) Primary Growth Hormone Resistance (en, replaced) Primary GH Resistance (en, replaced) Growth Hormone Receptor Defect (en, replaced) Laron Dwarfism (en, replaced) Laron Type Dwarfism I (en, replaced) Growth Hormone Insensitivity Syndrome (en, replaced) X
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