|
Hemoglobin C Disease
|
C16.320.070.490 |
|
|
Ciliophora Infections
|
C01.610.752.200 |
|
|
Occipital Lobe
|
A08.186.211.200.885.287.500.571 |
|
|
Skin Absorption
|
G03.787.024.500.750 |
|
|
Neurocutaneous Syndromes
|
C16.131.831.350.712 |
|
|
Receptor, Serotonin, 5-HT1B
|
D12.776.543.750.720.670.100.500 |
|
|
Autoreceptors
|
D12.776.543.750.720.670.100 |
|
|
Estrone
|
D06.472.334.851.437.996 |
|
|
Estrogens, Esterified (USP)
|
D06.472.334.851.437.994 |
|
|
NF-kappa B p52 Subunit
|
D12.776.930.600.186 |
|
|
Fertility
|
D005298 |
[The capacity to conceive or to induce conception. It may refer to either the male or female.
] |
|
Fertility Agents
|
D005299 |
[Drugs used to increase fertility or to treat infertility.
] |
|
Dysplastic Nevus Syndrome
|
C04.557.665.560.260 |
|
|
Classical Lissencephalies and Subcortical Band Heterotopias
|
D054221 |
[Disorders comprising a spectrum of brain malformations representing the paradigm of a diffuse neuronal migration disorder. They result in cognitive impairment; SEIZURES; and HYPOTONIA or spasticity. Mutations of two genes, LIS1, the gene for the non-catalytic subunit of PLATELET-ACTIVATING FACTOR ACETYLHYDROLASE IB; and DCX or XLIS, the gene for doublecortin, have been identified as the most common causes of disorders in this spectrum. Additional variants of classical (Type I) lissencephaly have been linked to RELN, the gene for reelin, and ARX, the gene for aristaless related homeobox protein. (From Leventer, R.J., et al, Mol Med Today. 2000 Jul;6(7):277-84 and Barkovich, A.J., et al, Neurology. 2005 Dec 27;65(12):1873-87.)
] |
|
Organothiophosphates
|
D02.705.539.345 |
|
|
Organothiophosphorus Compounds
|
D02.705.539 |
|
|
Cobblestone Lissencephaly
|
D054222 |
[The smooth pebbled appearance of the CEREBRAL CORTEX with a thickened cortex and reduced and abnormal white matter, which results from migration of heterotopic neurons beyond the marginal zone into the leptomeninges through gaps in the external BASEMENT MEMBRANE. There is also enlarged ventricles, underdeveloped BRAINSTEM and cerebellum, and absence of the CORPUS CALLOSUM. These abnormalities occur as a syndrome without other birth defects (cobblestone complex) or in other syndromes associated with congenital MUSCULAR DYSTROPHY, often involving the eye, such as the Walker-Warburg Syndrome, Fukuyama congenital muscular dystrophy, and muscle-eye-brain disease.
] |
|
Automation
|
J01.897.104 |
|
|
Dental Clasps
|
E07.695.190.180 |
|
|
Malformations of Cortical Development
|
D054220 |
[Abnormalities in the development of the CEREBRAL CORTEX. These include malformations arising from abnormal neuronal and glial CELL PROLIFERATION or APOPTOSIS (Group I); abnormal neuronal migration (Group II); and abnormal establishment of cortical organization (Group III). Many INBORN METABOLIC BRAIN DISORDERS affecting CNS formation are often associated with cortical malformations. They are common causes of EPILEPSY and developmental delay.
] |
