|
Cubital Tunnel Syndrome
|
C26.844.150.957.200 |
|
|
Ulnar Nerve Compression Syndromes
|
C26.844.150.957 |
|
|
Haemophilus paraphrophilus
|
D044136 |
[A species of gram-negative bacteria in the genus HAEMOPHILUS, found in the normal flora of the human ORAL CAVITY and PHARYNX. It can cause SUBACUTE BACTERIAL ENDOCARDITIS; and BRAIN ABSCESS, among other conditions.
] |
|
Racepinephrine
|
D02.033.100.291.310.500 |
|
|
Epinephrine
|
D02.033.100.291.310 |
|
|
Haemophilus parasuis
|
D044137 |
[A species of gram-negative bacteria in the genus HAEMOPHILUS found, in the normal upper respiratory tract of SWINE.
] |
|
Lobbying
|
I01.738.610 |
|
|
Haemophilus somnus
|
D044138 |
[A species of gram-negative bacteria (currently incertae sedis) causing multisystem disease in CATTLE.
] |
|
Nocturnal Myoclonus Syndrome
|
D020189 |
[Excessive periodic leg movements during sleep that cause micro-arousals and interfere with the maintenance of sleep. This condition induces a state of relative sleep deprivation which manifests as excessive daytime hypersomnolence. The movements are characterized by repetitive contractions of the tibialis anterior muscle, extension of the toe, and intermittent flexion of the hip, knee and ankle. (Adams et al., Principles of Neurology, 6th ed, p387)
] |
|
Phosphotransferases (Nitrogenous Group Acceptor)
|
D08.811.913.696.640 |
|
|
Receptor, Angiotensin, Type 2
|
D044139 |
[An angiotensin receptor subtype that is expressed at high levels in fetal tissues. Many effects of the angiotensin type 2 receptor such as VASODILATION and sodium loss are the opposite of that of the ANGIOTENSIN TYPE 1 RECEPTOR.
] |
|
Adenosine Triphosphate
|
D13.695.827.068.236 |
|
|
Simendan
|
D02.442.288.610 |
|
|
Canthaxanthin
|
D02.455.426.392.368.367.379.249.887.249 |
|
|
Leukodystrophy, Globoid Cell
|
C16.320.565.189.362.500 |
|
|
Myoclonic Epilepsy, Juvenile
|
D020190 |
[A disorder characterized by the onset of myoclonus in adolescence, a marked increase in the incidence of absence seizures (see EPILEPSY, ABSENCE), and generalized major motor seizures (see EPILEPSY, TONIC-CLONIC). The myoclonic episodes tend to occur shortly after awakening. Seizures tend to be aggravated by sleep deprivation and alcohol consumption. Hereditary and sporadic forms have been identified. (From Adams et al., Principles of Neurology, 6th ed, p323)
] |
|
Myoclonic Epilepsies, Progressive
|
D020191 |
[A heterogeneous group of primarily familial EPILEPSY disorders characterized by myoclonic seizures, tonic-clonic seizures, ataxia, progressive intellectual deterioration, and neuronal degeneration. These include LAFORA DISEASE; MERRF SYNDROME; NEURONAL CEROID-LIPOFUSCINOSIS; sialidosis (see MUCOLIPIDOSES), and UNVERRICHT-LUNDBORG SYNDROME.
] |
|
Paxillin
|
D12.776.512.374 |
|
|
Evolution, Molecular
|
D019143 |
[The process of cumulative change at the level of DNA; RNA; and PROTEINS, over successive generations.
] |
|
Tomatine
|
D03.132.760.864 |
|
