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Items: 15

1.

ANGIOTENSIN I-CONVERTING ENZYME INSERTION/DELETION POLYMORPHISM

MedGen UID:
864224
Concept ID:
C4015787
Finding
2.

ALZHEIMER DISEASE, PROTECTION AGAINST

MedGen UID:
762362
Concept ID:
C3549448
Disease or Syndrome
3.

Alzheimer disease, early-onset, with cerebral amyloid angiopathy

MedGen UID:
400198
Concept ID:
C1863053
Disease or Syndrome
4.

STROKE, HEMORRHAGIC, SUSCEPTIBILITY TO

MedGen UID:
400151
Concept ID:
C1862876
Finding
5.

Microvascular complications of diabetes 3

MedGen UID:
390806
Concept ID:
C2675470
Finding
6.

Alzheimer disease, type 1

MedGen UID:
354892
Concept ID:
C1863052
Disease or Syndrome
7.

Severe acute respiratory syndrome, progression of

MedGen UID:
354854
Concept ID:
C1862877
Finding
8.

Susceptibility to progression to renal failure in IgA nephropathy

MedGen UID:
349625
Concept ID:
C1862886
Finding
9.

Angiotensin i-converting enzyme, benign serum increase

MedGen UID:
349623
Concept ID:
C1862874
Finding
10.

ANGIOTENSIN I-CONVERTING ENZYME, PLASMA LEVEL OF

MedGen UID:
349622
Concept ID:
C1862873
Finding
11.

STROKE, ISCHEMIC, SUSCEPTIBILITY TO

MedGen UID:
347320
Concept ID:
C1856857
Finding
12.

Presenile And Senile Dementia

MedGen UID:
323817
Concept ID:
C1541844
Mental or Behavioral Dysfunction
13.

MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO

MedGen UID:
318680
Concept ID:
C1832662
Finding
14.

Renal dysplasia

Autosomal recessive renal tubular dysgenesis is a severe disorder of renal tubular development characterized by persistent fetal anuria and perinatal death, probably due to pulmonary hypoplasia from early-onset oligohydramnios (the Potter phenotype) (Gribouval et al., 2005). Absence or paucity of differentiated proximal tubules is the histopathologic hallmark of the disorder and may be associated with skull ossification defects. [from GTR]

MedGen UID:
82738
Concept ID:
C0266313
Disease or Syndrome
15.

Alzheimer disease

Alzheimer disease (AD) is characterized by dementia that typically begins with subtle and poorly recognized failure of memory and slowly becomes more severe and, eventually, incapacitating. Other common findings include confusion, poor judgment, language disturbance, agitation, withdrawal, and hallucinations. Occasionally, seizures, Parkinsonian features, increased muscle tone, myoclonus, incontinence, and mutism occur. Death usually results from general inanition, malnutrition, and pneumonia. The typical clinical duration of the disease is eight to ten years, with a range from one to 25 years. Approximately 25% of all AD is familial (i.e., =2 persons in a family have AD) of which approximately 95% is late onset (age >60-65 years) and 5% is early onset (age <65 years). [from GTR]

MedGen UID:
1853
Concept ID:
C0002395
Disease or Syndrome
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