Butterfly-shaped pigmentary macular dystrophy
|
disease |
|
Disease or Syndrome
|
7
|
|
0.010 |
None |
1.000 |
1 |
|
1996 |
1996 |
Rod dystrophy
|
disease |
|
Disease or Syndrome
|
2
|
2
|
0.010 |
None |
1.000 |
1 |
|
1996 |
1996 |
Cone Dystrophy
|
disease |
Eye Diseases
|
Disease or Syndrome
|
48
|
31
|
0.010 |
None |
1.000 |
1 |
|
1997 |
1997 |
Carcinogenesis
|
phenotype |
Pathological Conditions, Signs and Symptoms; Neoplasms
|
Neoplastic Process
|
6243
|
355
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Blindness
|
phenotype |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
393
|
34
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
Infant, Extremely Low Birth Weight
|
phenotype |
|
Disease or Syndrome
|
15
|
1
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Dominant drusen
|
disease |
|
Congenital Abnormality
|
4
|
2
|
0.010 |
None |
1.000 |
1 |
|
2002 |
2002 |
Shwachman syndrome
|
disease |
|
Disease or Syndrome
|
49
|
13
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Intussusception of rectum
|
phenotype |
Digestive System Diseases
|
Acquired Abnormality
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
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 |
Malnutrition
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
417
|
29
|
0.010 |
None |
1.000 |
1 |
|
2014 |
2014 |
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 |
Rectocele
|
phenotype |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
|
Acquired Abnormality
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
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 |
Respiratory Distress Syndrome
|
disease |
|
Disease or Syndrome
|
58
|
9
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Sleeplessness
|
phenotype |
Nervous System Diseases; Mental Disorders
|
Sign or Symptom
|
174
|
30
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus
|
disease |
|
Disease or Syndrome
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Major Congenital Anomaly
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Pauci-immune Glomerulonephritis associated with Granulomatosis with Polyangiitis
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
71
|
15
|
0.010 |
None |
1.000 |
1 |
|
2005 |
2005 |
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 |
Somnolence
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Mental or Behavioral Dysfunction
|
87
|
8
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Steroid Sulfatase Deficiency Disease
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
181
|
5
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
STARGARDT DISEASE 1 (disorder)
|
disease |
|
Disease or Syndrome
|
23
|
317
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |