Elliptocytosis, Hereditary
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Disease or Syndrome
23
1
0.420
None
1.000
3
1991
2001
Atrial Fibrillation
disease
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
Disease or Syndrome
939
584
0.400
None
1.000
2
1
2018
2018
Malaria
disease
Infections
Disease or Syndrome
685
148
0.320
None
1.000
2
2001
2004
Persistent atrial fibrillation
phenotype
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
Pathologic Function
156
0.300
None
1.000
2
2018
2018
familial atrial fibrillation
phenotype
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
Pathologic Function
157
1
0.300
None
1.000
2
2018
2018
Paroxysmal atrial fibrillation
disease
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
Disease or Syndrome
226
8
0.300
None
1.000
2
2018
2018
stomatocytic anemia
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
15
1
0.100
None
0
Splenomegaly
phenotype
Pathological Conditions, Signs and Symptoms
Finding
345
19
0.100
None
0
Chills
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
34
0.100
None
0
Reticulocytosis
phenotype
Pathological Conditions, Signs and Symptoms
Finding
40
1
0.100
None
0
Frontal bossing
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Congenital Abnormality
321
22
0.100
None
0
Elliptocytosis found
phenotype
Finding
12
0.100
None
0
Stomatocytosis Result
phenotype
Laboratory or Test Result
13
0.100
None
0
Hyperbilirubinemia, Neonatal
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Disease or Syndrome
33
15
0.100
None
0
Increased red cell osmotic fragility
phenotype
Finding
9
0.100
None
0
Prolonged neonatal jaundice
phenotype
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Finding
59
14
0.100
None
0
Postnatal growth retardation
phenotype
Finding
121
11
0.100
None
0
GERBICH BLOOD GROUP SYSTEM, GERBICH PHENOTYPE
phenotype
Finding
1
1
0.100
None
0
1
Cholelithiasis
disease
Digestive System Diseases
Disease or Syndrome
252
90
0.100
None
0
Abdominal Pain
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
302
18
0.100
None
0
Anemia, Hemolytic, Congenital
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Disease or Syndrome
27
8
0.100
None
0
×
CUI:
C0015967
Disease:
Fever
Fever
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
1021
66
0.100
None
0
Hydrops Fetalis
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases
Disease or Syndrome
92
14
0.100
None
0
Tumor Cell Invasion
phenotype
Neoplastic Process
6626
169
0.030
None
1.000
3
1996
2008
Seizures
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
2152
553
0.020
None
1.000
2
2017
2018