ONKI3 | Medical Subject Headings

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The way property values are displayed: value/row values side by side

The way concept relations are shown: separately in hierarchy

Dwarfism, Pituitary

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Dwarfism ∟ Dwarfism, Pituitary 9 coordinate concepts ∟ Acromegaly \| ∟ Congenital Hypothyroidism \| ∟ Gigantism \| ∟ Osteitis Fibrosa Cystica \| ∟ Achondroplasia \| ∟ Cockayne Syndrome \| ∟ Laron Syndrome \| ∟ Mulibrey Nanism \| ∟ Thanatophoric Dysplasia Medical Subject Headings (MeSH) ∟ Endocrine System Diseases ∟ Dwarfism ∟ Dwarfism, Pituitary 9 coordinate concepts ∟ Acromegaly \| ∟ Congenital Hypothyroidism \| ∟ Gigantism \| ∟ Osteitis Fibrosa Cystica \| ∟ Achondroplasia \| ∟ Cockayne Syndrome \| ∟ Laron Syndrome \| ∟ Mulibrey Nanism \| ∟ Thanatophoric Dysplasia Medical Subject Headings (MeSH) ∟ Endocrine System Diseases ∟ Pituitary Diseases ∟ Hypopituitarism ∟ Dwarfism, Pituitary 9 coordinate concepts ∟ Acromegaly \| ∟ Congenital Hypothyroidism \| ∟ Gigantism \| ∟ Osteitis Fibrosa Cystica \| ∟ Achondroplasia \| ∟ Cockayne Syndrome \| ∟ Laron Syndrome \| ∟ Mulibrey Nanism \| ∟ Thanatophoric Dysplasia Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Developmental ∟ Dwarfism ∟ Dwarfism, Pituitary 9 coordinate concepts ∟ Acromegaly \| ∟ Congenital Hypothyroidism \| ∟ Gigantism \| ∟ Osteitis Fibrosa Cystica \| ∟ Achondroplasia \| ∟ Cockayne Syndrome \| ∟ Laron Syndrome \| ∟ Mulibrey Nanism \| ∟ Thanatophoric Dysplasia Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Endocrine ∟ Dwarfism, Pituitary 9 coordinate concepts ∟ Acromegaly \| ∟ Congenital Hypothyroidism \| ∟ Gigantism \| ∟ Osteitis Fibrosa Cystica \| ∟ Achondroplasia \| ∟ Cockayne Syndrome \| ∟ Laron Syndrome \| ∟ Mulibrey Nanism \| ∟ Thanatophoric Dysplasia Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Hypothalamic Diseases ∟ Pituitary Diseases ∟ Hypopituitarism ∟ Dwarfism, Pituitary 9 coordinate concepts ∟ Acromegaly \| ∟ Congenital Hypothyroidism \| ∟ Gigantism \| ∟ Osteitis Fibrosa Cystica \| ∟ Achondroplasia \| ∟ Cockayne Syndrome \| ∟ Laron Syndrome \| ∟ Mulibrey Nanism \| ∟ Thanatophoric Dysplasia X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Dwarfism ∟ Dwarfism, Pituitary Medical Subject Headings (MeSH) ∟ Endocrine System Diseases ∟ Dwarfism ∟ Dwarfism, Pituitary Medical Subject Headings (MeSH) ∟ Endocrine System Diseases ∟ Pituitary Diseases ∟ Hypopituitarism ∟ Dwarfism, Pituitary Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Developmental ∟ Dwarfism ∟ Dwarfism, Pituitary Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Endocrine ∟ Dwarfism, Pituitary Medical Subject Headings (MeSH) ∟ Nervous System Diseases ∟ Central Nervous System Diseases ∟ Brain Diseases ∟ Hypothalamic Diseases ∟ Pituitary Diseases ∟ Hypopituitarism ∟ Dwarfism, Pituitary Dwarfism > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Dwarfism > Endocrine System Diseases > Medical Subject Headings (MeSH) Hypopituitarism > Pituitary Diseases > Endocrine System Diseases > Medical Subject Headings (MeSH) Dwarfism > Bone Diseases, Developmental > Bone Diseases > Musculoskeletal Diseases > Medical Subject Headings (MeSH) Bone Diseases, Endocrine > Bone Diseases > Musculoskeletal Diseases > Medical Subject Headings (MeSH) Hypopituitarism > Pituitary Diseases > Hypothalamic Diseases > Brain Diseases > Central Nervous System Diseases > Nervous System Diseases > Medical Subject Headings (MeSH) X
Scope note:	A form of dwarfism caused by complete or partial GROWTH HORMONE deficiency, resulting from either the lack of GROWTH HORMONE-RELEASING FACTOR from the HYPOTHALAMUS or from the mutations in the growth hormone gene (GH1) in the PITUITARY GLAND. It is also known as Type I pituitary dwarfism. Human hypophysial dwarf is caused by a deficiency of HUMAN GROWTH HORMONE during development. X
activeMeSHYear*:	2006 \| 2007X
dateCreated*:	1999-01-01X
dateRevised*:	2005-06-30X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Acromegaly \| Congenital Hypothyroidism \| Gigantism \| Osteitis Fibrosa Cystica \| Achondroplasia \| Cockayne Syndrome \| Laron Syndrome \| Mulibrey Nanism \| Thanatophoric Dysplasia X
URI:	X
Labels and equivalent concepts:	Aivolisäkeperäinen lyhytkasvuisuus (fi) Pituitaarinen kääpiökasvuisuus (fi, replaced) Pituitaarinen lyhytkasvuisuus (fi, replaced) Aivolisäkeperäinen kääpiökasvuisuus (fi, replaced) Dvärgväxt, hypofysär (sv) Hypofysär dvärgväxt (sv, replaced) Pituitary Dwarf (en, replaced) Growth Hormone Deficiency Dwarfism (en, replaced) Hyposomatotrophic Dwarfism (en, replaced) Nanism, Pituitary (en, replaced) Dwarfism, Growth Hormone Deficiency (en, replaced) Nanosomia pituitaria (la-FI, replaced) X
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