Megaloblastic Anemia 1
disease
Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Hemic and Lymphatic Diseases
Disease or Syndrome
9
68
0.770
None
1.000
13
25
2003
2018
Adrenoleukodystrophy
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Endocrine System Diseases
Disease or Syndrome
294
116
0.080
None
1.000
8
1981
2019
Adrenomyeloneuropathy
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Endocrine System Diseases
Disease or Syndrome
38
2
0.030
None
1.000
3
1990
2015
Malabsorption Syndrome
group
Digestive System Diseases; Nutritional and Metabolic Diseases
Disease or Syndrome
239
0.020
None
1.000
2
2003
2011
Anemia, Megaloblastic
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
26
2
0.120
None
1.000
2
1
2003
2005
Megaloblastic anemia due to inborn errors of metabolism
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
3
0.300
None
1.000
2
2011
2015
Spinal Cord Diseases
group
Nervous System Diseases
Disease or Syndrome
84
3
0.020
None
1.000
2
2008
2015
Neurogenic Inflammation
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Injury or Poisoning
18
0.300
None
1.000
2
2006
2007
Color blindness
disease
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
Disease or Syndrome
33
4
0.010
None
1.000
1
1990
1990
Somatotropin deficiency
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases
Disease or Syndrome
154
14
0.010
None
1.000
1
2014
2014
Congenital neurologic anomalies
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Congenital Abnormality
84
4
0.010
None
1.000
1
2007
2007
Anasarca
phenotype
Pathological Conditions, Signs and Symptoms
Pathologic Function
41
0.300
None
1.000
1
2007
2007
Carcinogenesis
phenotype
Pathological Conditions, Signs and Symptoms; Neoplasms
Neoplastic Process
6243
355
0.010
None
1.000
1
2009
2009
Disorder of macula of retina
group
Eye Diseases
Disease or Syndrome
49
24
0.010
None
1.000
1
2018
2018
Intrinsic Factor Deficiency
disease
Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
Disease or Syndrome
18
6
0.010
None
1.000
1
2012
2012
Benign melanocytic nevus
disease
Neoplasms
Neoplastic Process
122
20
0.010
None
1.000
1
2006
2006
Acute Kidney Insufficiency
disease
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
104
0.300
None
1.000
1
2011
2011
HYPERCHOLESTEROLEMIA, AUTOSOMAL RECESSIVE
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
19
9
0.010
None
1.000
1
2010
2010
Acute kidney injury
disease
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Injury or Poisoning
185
3
0.300
None
1.000
1
2011
2011
Isolated somatotropin deficiency
disease
Disease or Syndrome
168
27
0.010
None
1.000
1
2014
2014
×
CUI:
C0013604
Disease:
Edema
Edema
phenotype
Pathological Conditions, Signs and Symptoms
Pathologic Function
126
1
0.300
None
1.000
1
2007
2007
Tracheal Diseases
group
Respiratory Tract Diseases
Disease or Syndrome
155
1
0.010
None
1.000
1
1990
1990
Bone Marrow Diseases
group
Hemic and Lymphatic Diseases
Disease or Syndrome
84
3
0.010
None
1.000
1
2015
2015
Color vision defect
phenotype
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
Disease or Syndrome
94
4
0.010
None
1.000
1
1990
1990
Cystic Fibrosis
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases
Disease or Syndrome
852
704
0.010
None
1.000
1
1990
1990