All terms in HP

Label Id Description
Hypokalemic hypochloremic metabolic alkalosis HP_0004909
Hypochloremic metabolic alkalosis HP_0005977
Hypokalemic metabolic alkalosis HP_0001960
broad ligament of uterus UBERON_0012332 [A broad fold of peritoneum that extends from the side of the uterus to the wall of the pelvis.]
ligament UBERON_0000211 [Dense regular connective tissue connecting two or more adjacent skeletal elements or supporting an organ.]
Hypernatremic dehydration HP_0004906
Hypertonic dehydration HP_0001986
nasal-associated lymphoid tissue UBERON_0012330 [The lymphocytic cell population present in the mucosa of the nasopharyngeal duct of some animals.]
mucosa-associated lymphoid tissue UBERON_0001961 [Diffuse system of small concentrations of lymphoid tissue found in various sites of the body such as the gastrointestinal tract, thyroid, breast, lung, salivary glands, eye, and skin[WP]. Mucosal-associated lymphoid tissue is typically found as nodules associated with mucosal epithelia with distinct internal structures including B- and T-zones for the activation of lymphocytes[GO].]
gut-associated lymphoid tissue UBERON_0001962 [Mucosa-associated lymphoid tissue in digestive tract. includes Peyer's patches, appendix, and solitary lymph nodules[GO].]
Maturity-onset diabetes of the young HP_0004904 [The term Maturity-onset diabetes of the young (MODY) was initially used for patients diagnosed with fasting hyperglycemia that could be treated without insulin for more than two years, where the initial diagnosis was made at a young age (under 25 years). Thus, MODY combines characteristics of type 1 diabetes (young age at diagnosis) and type 2 diabetes (less insulin dependence than type 1 diabetes). The term MODY is now most often used to refer to a group of monogenic diseases with these characteristics. Here, the term is used to describe hyperglycemia diagnosed at a young age with no or minor insulin dependency, no evidence of insulin resistance, and lack of evidence of autoimmune destruction of the beta cells.]
Diabetes mellitus HP_0000819 [A group of abnormalities characterized by hyperglycemia and glucose intolerance.]
Reduced circulating vitamin A concentration HP_0004905 [Concentration of vitamin A below the lower limit of normal in the blood circulation.]
Abnormal circulating vitamin A concentration HP_0008372 [Concentration of vitamin A in the blood circulation outside limits of normal.]
Congenital lactic acidosis HP_0004902 [A form of lactic acidemia with congenital onset.]
Episodic metabolic acidosis HP_0004911 [Repeated transient episodes of metabolic acidosis, that is, of the buildup of acid or depletion of base due to accumulation of metabolic acids.]
Metabolic acidosis HP_0001942 [Metabolic acidosis (MA) is characterized by a fall in blood pH due to a reduction of serum bicarbonate concentration. This can occur as a result of either the accumulation of acids (high anion gap MA) or the loss of bicarbonate from the gastrointestinal tract or the kidney (hyperchloremic MA). By definition, MA is not due to a respirary cause.]
Hypophosphatemic rickets HP_0004912
Hypophosphatemia HP_0002148 [An abnormally decreased phosphate concentration in the blood.]
Rickets HP_0002748 [Rickets is divided into two major categories including calcipenic and phosphopenic. Hypophosphatemia is described as a common manifestation of both categories. Hypophosphatemic rickets is the most common type of rickets that is characterized by low levels of serum phosphate, resistance to ultraviolet radiation or vitamin D intake. There are several issues involved in hypophosphatemic rickets such as calcium, vitamin D, phosphorus deficiencies. Moreover, other disorder can be associated with its occurrence such as absorption defects due to pancreatic, intestinal, gastric, and renal disorders and hepatobiliary disease. Symptoms are usually seen in childhood and can be varied in severity. Severe forms may be linked to bowing of the legs, poor bone growth, and short stature as well as joint and bone pain. Hypophosphatemic rickets are associated with renal excretion of phosphate, hypophosphatemia, and mineral defects in bones. The familial type of the disease is the most common type of rickets.]