Hereditary macular dystrophy
|
disease |
|
Congenital Abnormality
|
39
|
10
|
0.060 |
None |
1.000 |
6 |
|
1993 |
2009 |
Stargardt's disease
|
phenotype |
|
Disease or Syndrome
|
45
|
24
|
0.020 |
None |
1.000 |
2 |
|
2007 |
2007 |
Tuberculin (skin test) positive
|
disease |
|
Disease or Syndrome
|
3
|
|
0.020 |
None |
1.000 |
2 |
|
2011 |
2017 |
Red Blood Cell Count measurement
|
phenotype |
|
Laboratory Procedure
|
717
|
1599
|
0.100 |
None |
1.000 |
1 |
1
|
2009 |
2009 |
Violence
|
phenotype |
|
Mental or Behavioral Dysfunction
|
70
|
6
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Caffeine related disorders
|
group |
|
Mental or Behavioral Dysfunction
|
360
|
56
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Shwachman syndrome
|
disease |
|
Disease or Syndrome
|
49
|
13
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Dominant drusen
|
disease |
|
Congenital Abnormality
|
4
|
2
|
0.010 |
None |
1.000 |
1 |
|
2002 |
2002 |
Infant, Extremely Low Birth Weight
|
phenotype |
|
Disease or Syndrome
|
15
|
1
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Rod dystrophy
|
disease |
|
Disease or Syndrome
|
2
|
2
|
0.010 |
None |
1.000 |
1 |
|
1996 |
1996 |
Respiratory Distress Syndrome
|
disease |
|
Disease or Syndrome
|
58
|
9
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Finding of Mean Corpuscular Hemoglobin
|
phenotype |
|
Finding
|
653
|
1206
|
0.100 |
None |
1.000 |
1 |
1
|
2019 |
2019 |
IMMUNE SUPPRESSION
|
phenotype |
|
Disease or Syndrome
|
222
|
3
|
0.010 |
None |
1.000 |
1 |
|
2020 |
2020 |
STARGARDT DISEASE 1 (disorder)
|
disease |
|
Disease or Syndrome
|
23
|
317
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus
|
disease |
|
Disease or Syndrome
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Butterfly-shaped pigmentary macular dystrophy
|
disease |
|
Disease or Syndrome
|
7
|
|
0.010 |
None |
1.000 |
1 |
|
1996 |
1996 |
Corpuscular Hemoglobin Concentration Mean
|
phenotype |
|
Laboratory or Test Result
|
401
|
4389
|
0.100 |
None |
1.000 |
1 |
6
|
2012 |
2012 |
Mental Depression
|
disease |
Behavior and Behavior Mechanisms
|
Mental or Behavioral Dysfunction
|
1478
|
271
|
0.020 |
None |
1.000 |
2 |
|
2017 |
2019 |
Depressed mood
|
phenotype |
Behavior and Behavior Mechanisms
|
Mental or Behavioral Dysfunction
|
1461
|
269
|
0.020 |
None |
1.000 |
2 |
|
2017 |
2019 |
Major Congenital Anomaly
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Retinitis Pigmentosa
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
546
|
541
|
0.100 |
None |
0.955 |
22 |
|
1991 |
2017 |
Autosomal dominant retinitis pigmentosa
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Congenital Abnormality
|
85
|
65
|
0.100 |
None |
1.000 |
22 |
|
1991 |
2009 |
Adult-Onset Vitelliform Macular Dystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
8
|
16
|
0.040 |
None |
1.000 |
4 |
|
1997 |
2008 |
Cone-Rod Dystrophy 2
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
254
|
51
|
0.030 |
None |
1.000 |
3 |
|
1996 |
1998 |
Cone-Rod Dystrophies
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
86
|
53
|
0.020 |
None |
1.000 |
2 |
|
1996 |
1998 |