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

Pseudohypoparathyroidism

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Metal Metabolism, Inborn Errors ∟ Pseudohypoparathyroidism 16 coordinate concepts 1 subordinate concept ∟ Pseudopseudohypoparathyroidism ∟ Hemochromatosis \| ∟ Hepatolenticular Degeneration \| ∟ Hypophosphatasia \| ∟ Hypophosphatemia, Familial \| ∟ Menkes Kinky Hair Syndrome \| ∟ Paralyses, Familial Periodic \| ∟ Bone Demineralization, Pathologic \| ∟ Mucolipidoses \| ∟ Osteomalacia \| ∟ Osteoporosis \| ∟ Renal Osteodystrophy \| ∟ Rickets \| ∟ Calcinosis \| ∟ Decalcification, Pathologic \| ∟ Hypercalcemia \| ∟ Hypocalcemia Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Metabolic ∟ Pseudohypoparathyroidism 16 coordinate concepts 1 subordinate concept ∟ Pseudopseudohypoparathyroidism ∟ Hemochromatosis \| ∟ Hepatolenticular Degeneration \| ∟ Hypophosphatasia \| ∟ Hypophosphatemia, Familial \| ∟ Menkes Kinky Hair Syndrome \| ∟ Paralyses, Familial Periodic \| ∟ Bone Demineralization, Pathologic \| ∟ Mucolipidoses \| ∟ Osteomalacia \| ∟ Osteoporosis \| ∟ Renal Osteodystrophy \| ∟ Rickets \| ∟ Calcinosis \| ∟ Decalcification, Pathologic \| ∟ Hypercalcemia \| ∟ Hypocalcemia Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Calcium Metabolism Disorders ∟ Pseudohypoparathyroidism 16 coordinate concepts 1 subordinate concept ∟ Pseudopseudohypoparathyroidism ∟ Hemochromatosis \| ∟ Hepatolenticular Degeneration \| ∟ Hypophosphatasia \| ∟ Hypophosphatemia, Familial \| ∟ Menkes Kinky Hair Syndrome \| ∟ Paralyses, Familial Periodic \| ∟ Bone Demineralization, Pathologic \| ∟ Mucolipidoses \| ∟ Osteomalacia \| ∟ Osteoporosis \| ∟ Renal Osteodystrophy \| ∟ Rickets \| ∟ Calcinosis \| ∟ Decalcification, Pathologic \| ∟ Hypercalcemia \| ∟ Hypocalcemia Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Metal Metabolism, Inborn Errors ∟ Pseudohypoparathyroidism 16 coordinate concepts 1 subordinate concept ∟ Pseudopseudohypoparathyroidism ∟ Hemochromatosis \| ∟ Hepatolenticular Degeneration \| ∟ Hypophosphatasia \| ∟ Hypophosphatemia, Familial \| ∟ Menkes Kinky Hair Syndrome \| ∟ Paralyses, Familial Periodic \| ∟ Bone Demineralization, Pathologic \| ∟ Mucolipidoses \| ∟ Osteomalacia \| ∟ Osteoporosis \| ∟ Renal Osteodystrophy \| ∟ Rickets \| ∟ Calcinosis \| ∟ Decalcification, Pathologic \| ∟ Hypercalcemia \| ∟ Hypocalcemia X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Metal Metabolism, Inborn Errors ∟ Pseudohypoparathyroidism Medical Subject Headings (MeSH) ∟ Musculoskeletal Diseases ∟ Bone Diseases ∟ Bone Diseases, Metabolic ∟ Pseudohypoparathyroidism Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Calcium Metabolism Disorders ∟ Pseudohypoparathyroidism Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Metal Metabolism, Inborn Errors ∟ Pseudohypoparathyroidism Metal Metabolism, Inborn Errors > Metabolism, Inborn Errors > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Bone Diseases, Metabolic > Bone Diseases > Musculoskeletal Diseases > Medical Subject Headings (MeSH) Calcium Metabolism Disorders > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Metal Metabolism, Inborn Errors > Metabolism, Inborn Errors > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	Pseudopseudohypoparathyroidism X
Annotation:	a metab bone dis; do not confuse with PSEUDOPSEUDOHYPOPARATHYROIDISM X
historyNote*:	65(63) X
publicMeSHNote*:	65 X
Scope note:	A hereditary condition clinically resembling HYPOPARATHYROIDISM, but caused by failure of response to rather than deficiency of parathyroid hormones. It is characterized by hypocalcemia and hyperphosphatemia, and is commonly associated with short stature, obesity, short metacarpals, and ectopic calcification. (Dorland, 27th ed) X
activeMeSHYear*:	2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1965-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Hemochromatosis \| Hepatolenticular Degeneration \| Hypophosphatasia \| Hypophosphatemia, Familial \| Menkes Kinky Hair Syndrome \| Paralyses, Familial Periodic \| Bone Demineralization, Pathologic \| Mucolipidoses \| Osteomalacia \| Osteoporosis \| Renal Osteodystrophy \| Rickets \| Calcinosis \| Decalcification, Pathologic \| Hypercalcemia \| Hypocalcemia X
URI:	X
Labels and equivalent concepts:	Pseudohypoparatyreoosi (fi) Pseudohypoparatyreoidismi (fi, replaced) Pseudohypoparatyreos (sv) Pseudohypoparathyroidismus (la-FI, replaced) Pseudohypoparathyreosis (la-FI, replaced) X
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