MEGALOBLASTIC ANEMIA 1, NORWEGIAN TYPE
disease
Finding
1
2
0.100
None
0
2
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
Malabsorption of Vitamin B12
phenotype
Finding
3
0.100
None
0
Extravasation of Contrast Media
phenotype
Pathological Conditions, Signs and Symptoms; Wounds and Injuries
Pathologic Function
6
0.300
None
1.000
1
2007
2007
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
Neurogenic Inflammation
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Injury or Poisoning
18
0.300
None
1.000
2
2006
2007
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
HYPERCHOLESTEROLEMIA, AUTOSOMAL RECESSIVE
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
19
9
0.010
None
1.000
1
2010
2010
Anemia, Megaloblastic
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
26
2
0.120
None
1.000
2
1
2003
2005
Vitamin B 12 Deficiency
disease
Nutritional and Metabolic Diseases
Disease or Syndrome
29
11
0.100
None
0
1
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
Hypesthesia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
33
6
0.100
None
0
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
Anasarca
phenotype
Pathological Conditions, Signs and Symptoms
Pathologic Function
41
0.300
None
1.000
1
2007
2007
Disorder of macula of retina
group
Eye Diseases
Disease or Syndrome
49
24
0.010
None
1.000
1
2018
2018
Childhood onset
phenotype
Finding
56
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
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
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
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
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
Paresthesia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Disease or Syndrome
121
8
0.100
None
0
Benign melanocytic nevus
disease
Neoplasms
Neoplastic Process
122
20
0.010
None
1.000
1
2006
2006
×
CUI:
C0027960
Disease:
Nevus
Nevus
disease
Neoplasms
Neoplastic Process
125
43
0.010
None
1.000
1
2006
2006