| D003348 |
Cortisone |
A naturally occurring glucocorticoid that has been used in replacement therapy for ADRENAL INSUFFICIENCY and as an anti-inflammatory agent. Cortisone itself is inactive; it is converted in the liver to the active metabolite HYDROCORTISONE. (From Martindale, The Extra Pharmacopoeia, 30th ed, p726) |
17-Hydroxy-3,11,20-trioxopregn-4-en-21-yl acetate,Adreson,Cortisone Acetate,Cortone Acetate |
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| D000075262 |
Hypoadrenocorticism, Familial |
Hereditary forms of Addison disease that may exhibit autosomal recessive or X-linked inheritance. They are characterized by severe neurological symptoms, APNEA; and death in infancy. OMIM: 240200 |
AHC with Isolated Gonadotropin Deficiency,Addison Disease, X-Linked,Adrenal Hypoplasia, Congenital,Adrenal Hypoplasia, Congenital, with Hypogonadotropic Hypogonadism,Complex Glycerol Kinase Deficiency,Cytomegalic Adrenocortical Hypoplasia,Familial X-linked Addison Disease,X-linked Adrenal Hypoplasia,X-linked Congenital Adrenal Hypoplasia,Xp21 Contiguous Gene Deletion Syndrome,Addison Disease, X Linked,Adrenal Hypoplasia, X-linked,Congenital Adrenal Hypoplasia,Congenital Adrenal Hypoplasias,Cytomegalic Adrenocortical Hypoplasias,Familial Hypoadrenocorticism,Familial Hypoadrenocorticisms,Familial X linked Addison Disease,Hypoadrenocorticisms, Familial,Hypoplasia, Congenital Adrenal,X linked Adrenal Hypoplasia,X linked Congenital Adrenal Hypoplasia,X-Linked Addison Disease |
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| D000224 |
Addison Disease |
An adrenal disease characterized by the progressive destruction of the ADRENAL CORTEX, resulting in insufficient production of ALDOSTERONE and HYDROCORTISONE. Clinical symptoms include ANOREXIA; NAUSEA; WEIGHT LOSS; MUSCLE WEAKNESS; and HYPERPIGMENTATION of the SKIN due to increase in circulating levels of ACTH precursor hormone which stimulates MELANOCYTES. |
Addison's Disease,Primary Adrenal Insufficiency,Primary Adrenocortical Insufficiency,Primary Hypoadrenalism,Addisons Disease,Adrenal Insufficiency, Primary,Adrenocortical Insufficiencies, Primary,Adrenocortical Insufficiency, Primary,Disease, Addison,Hypoadrenalism, Primary,Hypoadrenalisms, Primary,Insufficiencies, Primary Adrenocortical,Insufficiency, Primary Adrenocortical,Primary Adrenocortical Insufficiencies |
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| D000305 |
Adrenal Cortex Hormones |
HORMONES produced by the ADRENAL CORTEX, including both steroid and peptide hormones. The major hormones produced are HYDROCORTISONE and ALDOSTERONE. |
Adrenal Cortex Hormone,Corticoid,Corticoids,Corticosteroid,Corticosteroids,Cortex Hormone, Adrenal,Hormone, Adrenal Cortex,Hormones, Adrenal Cortex |
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| D000309 |
Adrenal Insufficiency |
Conditions in which the production of adrenal CORTICOSTEROIDS falls below the requirement of the body. Adrenal insufficiency can be caused by defects in the ADRENAL GLANDS, the PITUITARY GLAND, or the HYPOTHALAMUS. |
Adrenal Gland Hypofunction,Hypoadrenalism,Adrenal Insufficiencies,Hypofunction, Adrenal Gland |
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| D001168 |
Arthritis |
Acute or chronic inflammation of JOINTS. |
Oligoarthritis,Polyarthritis,Arthritides,Oligoarthritides,Polyarthritides |
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| D001172 |
Arthritis, Rheumatoid |
A chronic systemic disease, primarily of the joints, marked by inflammatory changes in the synovial membranes and articular structures, widespread fibrinoid degeneration of the collagen fibers in mesenchymal tissues, and by atrophy and rarefaction of bony structures. Etiology is unknown, but autoimmune mechanisms have been implicated. |
Rheumatoid Arthritis |
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| D064791 |
Desoxycorticosterone Acetate |
The 21-acetate derivative of desoxycorticosterone. |
DOCA,DOC-21-acetate,Deoxycorticosterone-21-acetate,Desoxycorticosterone-21-acetate,Desoxycortone Acetate,Syncortyl,Acetate, Desoxycortone,DOC 21 acetate,Deoxycorticosterone 21 acetate,Desoxycorticosterone 21 acetate |
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