|
Styrenes
|
D02.455.426.559.389.150.750 |
|
|
Claudin-4
|
D12.776.543.940.200.400 |
|
|
Alkaline Phosphatase
|
D08.811.277.352.650.035 |
|
|
Phosphoric Monoester Hydrolases
|
D08.811.277.352.650 |
|
|
Encephalitis Virus, Eastern Equine
|
B04.820.230.150 |
|
|
Encephalitis Viruses
|
B04.820.230 |
|
|
Chemokine CCL19
|
D12.776.467.374.200.600.870 |
|
|
Macrophage Inflammatory Proteins
|
D12.776.467.374.200.600 |
|
|
alpha-Galactosidase
|
D08.811.277.450.410.050 |
|
|
Galactosidases
|
D08.811.277.450.410 |
|
|
Sweating, Gustatory
|
C10.177.825 |
|
|
Autonomic Nervous System Diseases
|
C10.177 |
|
|
Nucleotide Motifs
|
G05.360.080.611 |
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|
Base Sequence
|
G05.360.080 |
|
|
Myricaceae
|
B01.650.940.800.575.912.250.859.750.700 |
|
|
Multifocal Choroiditis
|
D000080364 |
[A multifocal uveitis syndrome involving the RETINAL PIGMENT EPITHELIUM and capillary layer of the CHOROID. It is characterized by chronic UVEITIS and multiple CHOROID lesions referred to as white dots, blurry vision, floaters, sensitivity to light, blind spots, and eye discomfort.
] |
|
White Dot Syndromes
|
D000080363 |
[A group of idiopathic multifocal posterior uveitis syndromes involving the CHOROID; RETINAL PIGMENT EPITHELIUM; and RETINA. They are characterized by multiple lesions of hypoautofluorescent dots in the FUNDUS OCULI and reduced VISUAL ACUITY. Several entities including BIRDSHOT CHORIORETINOPATHY are HLA-A ANTIGENS serotype A29 positive.
] |
|
Birdshot Chorioretinopathy
|
D000080365 |
[A form of chorioretinitis characterized by multiple small, cream-colored LESIONS, symmetrically scattered mainly around the OPTIC DISK. These lesions are the most distinctive sign and often appear at the level of the RETINAL PIGMENT EPITHELIUM but, on occasion, suggest an even deeper infiltration and may ultimately lead to visual loss. An association with HLA-A29 antigen (see HLA-A ANTIGENS) has been observed in nearly all patients.
] |
|
Stargardt Disease
|
D000080362 |
[A juvenile-onset macular dystrophy characterized by progressive loss of VISUAL ACUITY with normal acuity in peripheral VISUAL FIELDS. Other associated clinical features may include LIPOFUSCIN fundus autofluorescence, atrophy of the RETINAL PIGMENT EPITHELIUM, loss of color vision, PHOTOPHOBIA and PARACENTRAL SCOTOMA. Germline mutations in the ABCA4 gene have been identified in recessive and dominant diseases.
] |
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Nifuratel
|
D03.383.312.649.410 |
|
