|
Tuberculosis, Pleural
|
C08.528.928 |
|
|
Bufotenin
|
D03.633.100.473.914.237.150 |
|
|
N,N-Dimethyltryptamine
|
D03.633.100.473.914.237 |
|
|
Farber Lipogranulomatosis
|
C18.452.648.398.641.803.325 |
|
|
Postthrombotic Syndrome
|
D054070 |
[A condition caused by one or more episodes of DEEP VEIN THROMBOSIS, usually the blood clots are lodged in the legs. Clinical features include EDEMA; PAIN; aching; heaviness; and MUSCLE CRAMP in the leg. When severe leg swelling leads to skin breakdown, it is called venous STASIS ULCER.
] |
|
Cocarcinogenesis
|
C23.550.727.098.750 |
|
|
Hereditary Angioedema Type III
|
C14.907.079.500.500 |
|
|
Superior Sagittal Sinus
|
D054063 |
[The long large endothelium-lined venous channel on the top outer surface of the brain. It receives blood from a vein in the nasal cavity, runs backwards, and gradually increases in size as blood drains from veins of the brain and the DURA MATER. Near the lower back of the CRANIUM, the superior sagittal sinus deviates to one side (usually the right) and continues on as one of the TRANSVERSE SINUSES.
] |
|
Transverse Sinuses
|
D054064 |
[The two large endothelium-lined venous channels that begin at the internal occipital protuberance at the back and lower part of the CRANIUM and travels laterally and forward ending in the internal jugular vein (JUGULAR VEINS). One of the transverse sinuses, usually the right one, is the continuation of the SUPERIOR SAGITTAL SINUS. The other transverse sinus is the continuation of the straight sinus.
] |
|
Ischemic Contracture
|
D054061 |
[A type of permanent damage to muscles and nerves that results from prolonged lack blood flow to those tissues. It is characterized by shortening and stiffening of the muscles.
] |
|
Deaf-Blind Disorders
|
D054062 |
[The absence of both hearing and vision.
] |
|
alpha-Macroglobulins
|
D12.776.124.050.080 |
|
|
Dihydropyrimidine Dehydrogenase Deficiency
|
D054067 |
[An autosomal recessive disorder affecting DIHYDROPYRIMIDINE DEHYDROGENASE and causing familial pyrimidinemia. It is characterized by thymine-uraciluria in homozygous deficient patients. Even a partial deficiency in the enzyme leaves individuals at risk for developing severe 5-FLUOROURACIL-associated toxicity.
] |
|
Facial Nerve
|
A08.800.800.060.275 |
|
|
Livedo Reticularis
|
D054068 |
[A condition characterized by a reticular or fishnet pattern on the skin of lower extremities and other parts of the body. This red and blue pattern is due to deoxygenated blood in unstable dermal blood vessels. The condition is intensified by cold exposure and relieved by rewarming.
] |
|
Leukemia, Large Granular Lymphocytic
|
D054066 |
[A spectrum of disorders characterized by clonal expansions of the peripheral blood LYMPHOCYTE populations known as large granular lymphocytes which contain abundant cytoplasm and azurophilic granules. Subtypes develop from either CD3-negative NATURAL KILLER CELLS or CD3-positive T-CELLS. The clinical course of both subtypes can vary from spontaneous regression to progressive, malignant disease.
] |
|
Urobilin
|
D23.767.193.727 |
|
|
Multiple Acyl Coenzyme A Dehydrogenase Deficiency
|
D054069 |
[An autosomal recessive disorder of fatty acid oxidation, and branched chain amino acids (AMINO ACIDS, BRANCHED-CHAIN); LYSINE; and CHOLINE catabolism, that is due to defects in either subunit of ELECTRON TRANSFER FLAVOPROTEIN or its dehydrogenase, electron transfer flavoprotein-ubiquinone oxidoreductase (EC 1.5.5.1).
] |
|
Argon
|
D01.362.641.113 |
|
|
Gamma Rays
|
G01.750.250.300 |
|
