Amaurosis congenita of Leber, type 1
|
disease |
Eye Diseases
|
Disease or Syndrome
|
81
|
60
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Active tuberculosis
|
disease |
Infections
|
Disease or Syndrome
|
116
|
25
|
0.010 |
None |
1.000 |
1 |
|
2020 |
2020 |
Autosomal Recessive Polycystic Kidney Disease
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
69
|
317
|
0.010 |
None |
1.000 |
1 |
|
1998 |
1998 |
Pseudovaginal Perineoscrotal Hypospadias
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
8
|
42
|
0.010 |
None |
< 0.001 |
1 |
|
2019 |
2019 |
Violence
|
phenotype |
|
Mental or Behavioral Dysfunction
|
70
|
6
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Tuberculosis
|
disease |
Infections
|
Disease or Syndrome
|
1256
|
328
|
0.010 |
None |
1.000 |
1 |
|
2020 |
2020 |
Androgen-Insensitivity Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
247
|
176
|
0.010 |
None |
< 0.001 |
1 |
|
2019 |
2019 |
Infant, Extremely Low Birth Weight
|
phenotype |
|
Disease or Syndrome
|
15
|
1
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Respiratory Distress Syndrome, Adult
|
disease |
Respiratory Tract Diseases
|
Disease or Syndrome
|
434
|
60
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Pneumothorax
|
phenotype |
Respiratory Tract Diseases
|
Disease or Syndrome
|
69
|
3
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Clinical Chorioamnionitis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications
|
Disease or Syndrome
|
8
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Surfactant Dysfunction
|
disease |
Respiratory Tract Diseases
|
Disease or Syndrome
|
10
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Usher Syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
|
Disease or Syndrome
|
68
|
74
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |
PARKINSON DISEASE, LATE-ONSET
|
disease |
|
Disease or Syndrome
|
247
|
76
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |
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 |
1
|
2002 |
2002 |
Iron deficiency
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
179
|
13
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Caffeine related disorders
|
group |
|
Mental or Behavioral Dysfunction
|
360
|
56
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Leber Congenital Amaurosis
|
disease |
Eye Diseases
|
Disease or Syndrome
|
83
|
109
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |
5-Alpha Reductase Deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
8
|
5
|
0.010 |
None |
< 0.001 |
1 |
|
2019 |
2019 |
Transitory tachypnea of newborn
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
|
Disease or Syndrome
|
5
|
|
0.010 |
None |
1.000 |
1 |
|
2005 |
2005 |
orbit (eye disorders)
|
group |
Eye Diseases
|
Disease or Syndrome
|
64
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Carcinoma of larynx
|
disease |
Neoplasms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases
|
Neoplastic Process
|
456
|
65
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
RETINITIS PIGMENTOSA 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
32
|
21
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |
Usher Syndrome, Type I
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
|
Disease or Syndrome
|
23
|
168
|
0.010 |
None |
1.000 |
1 |
|
2012 |
2012 |