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Results: 12

1.

Viral Load result

The quantity of measurable virus in a body fluid. Change in viral load, measured in plasma, is sometimes used as a SURROGATE MARKER in disease progression. [from MeSH]

MedGen UID:
84035
Concept ID:
C0376705
Finding
2.

Neurosyphilis

Infections of the central nervous system caused by TREPONEMA PALLIDUM which present with a variety of clinical syndromes. The initial phase of infection usually causes a mild or asymptomatic meningeal reaction. The meningovascular form may present acutely as BRAIN INFARCTION. The infection may also remain subclinical for several years. Late syndromes include general paresis; TABES DORSALIS; meningeal syphilis; syphilitic OPTIC ATROPHY; and spinal syphilis. General paresis is characterized by progressive DEMENTIA; DYSARTHRIA; TREMOR; MYOCLONUS; SEIZURES; and Argyll-Robertson pupils. (Adams et al., Principles of Neurology, 6th ed, pp722-8) [from MeSH]

MedGen UID:
14360
Concept ID:
C0027927
Disease or Syndrome
3.

Immunodeficiency

MedGen UID:
505335
Concept ID:
CN002471
Finding
4.

Immunodeficiency

Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral. [from MeSH]

MedGen UID:
7034
Concept ID:
C0021051
Disease or Syndrome
5.

MedGen UID:
137992
Concept ID:
C0343686
6.

Asymptomatic neurosyphilis

MedGen UID:
102259
Concept ID:
C0153167
Disease or Syndrome
7.

Neurosyphilis, Symptomatic

MedGen UID:
99211
Concept ID:
C0494053
Disease or Syndrome
8.

Secondary neurosyphilis

MedGen UID:
83366
Concept ID:
C0343683
Disease or Syndrome
9.

Neurosyphilis, Juvenile

MedGen UID:
57780
Concept ID:
C0153132
Disease or Syndrome
10.

Antitreponemal agent

Agents used to treat infections with bacteria of the genus TREPONEMA. This includes SYPHILIS & YAWS. [from MeSH]

MedGen UID:
8145
Concept ID:
C0003446
Pharmacologic Substance
11.

CSF pleocytosis

MedGen UID:
489830
Concept ID:
C0742915
Finding
12.

May-Hegglin anomaly

MYH9-related disorders (MYH9RD) are characterized by large platelets (i.e., >20% of platelets >4 µm in diameter) and thrombocytopenia (platelet count <150x10(9)/L), both of which are present from birth. MYH9RD is variably associated with young-adult onset of progressive high-frequency sensorineural hearing loss, presenile cataract, and renal disease manifesting initially as glomerulonephritis. Before identification of the gene in which mutation is causative, MYH9, individuals with MYH9RD were diagnosed as having Epstein syndrome, Fechtner syndrome, May-Hegglin anomaly, or Sebastian syndrome based on the combination of different clinical findings at the time of diagnosis. However, the realization that they all have MYH9 mutations and that their clinical picture often worsens throughout life as a result of late onset of non-hematologic manifestations has led the four conditions to be regarded as one disorder, now known as MYH9RD. [from GeneReviews]

MedGen UID:
87410
Concept ID:
C0340978
Finding

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