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
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
Neurogenic Inflammation
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Injury or Poisoning
18
0.300
None
1.000
2
2006
2007
Anasarca
phenotype
Pathological Conditions, Signs and Symptoms
Pathologic Function
41
0.300
None
1.000
1
2007
2007
Extravasation of Contrast Media
phenotype
Pathological Conditions, Signs and Symptoms; Wounds and Injuries
Pathologic Function
6
0.300
None
1.000
1
2007
2007
×
CUI:
C0013604
Disease:
Edema
Edema
phenotype
Pathological Conditions, Signs and Symptoms
Pathologic Function
126
1
0.300
None
1.000
1
2007
2007
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
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
Kidney Failure, Acute
disease
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
826
32
0.300
None
1.000
1
2011
2011
Anemia, Megaloblastic
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
26
2
0.120
None
1.000
2
1
2003
2005
Childhood onset
phenotype
Finding
56
0.100
None
0
Malabsorption of Vitamin B12
phenotype
Finding
3
0.100
None
0
Confusion
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms
Mental or Behavioral Dysfunction
75
5
0.100
None
0
Hypesthesia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
33
6
0.100
None
0
Vitamin B 12 Deficiency
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
29
11
0.100
None
0
1
Proteinuria
phenotype
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Finding
239
20
0.100
None
0
Paresthesia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Disease or Syndrome
121
8
0.100
None
0
Dementia
disease
Nervous System Diseases; Mental Disorders
Mental or Behavioral Dysfunction
816
176
0.100
None
0
MEGALOBLASTIC ANEMIA 1, NORWEGIAN TYPE
disease
Finding
1
2
0.100
None
0
2
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
Spinal Cord Diseases
group
Nervous System Diseases
Disease or Syndrome
84
3
0.020
None
1.000
2
2008
2015
Bone Marrow Diseases
group
Hemic and Lymphatic Diseases
Disease or Syndrome
84
3
0.010
None
1.000
1
2015
2015
HYPERCHOLESTEROLEMIA, AUTOSOMAL RECESSIVE
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
19
9
0.010
None
1.000
1
2010
2010