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Factor X Deficiency
Factor X Deficiency
Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in both the intrinsic and ex...<br/>Year introduced: 1991(1975)
MeSH
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Hypoprothrombinemias
Hypoprothrombinemias
Absence or reduced levels of PROTHROMBIN in the blood.<br/>
MeSH
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Receptor, Parathyroid Hormone, Type 2
Receptor, Parathyroid Hormone, Type 2
A parathyroid hormone receptor subtype found in the BRAIN and the PANCREAS. It is a G-protein-coupled receptor with a ligand specificity that varies between homologs from diff...<br/>Year introduced: 2004
MeSH
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