GERBICH BLOOD GROUP SYSTEM, GERBICH PHENOTYPE
phenotype
Finding
1
1
0.100
None
0
1
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
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
Abdominal Pain
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
302
18
0.100
None
0
×
CUI:
C0015967
Disease:
Fever
Fever
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
1021
66
0.100
None
0
Cholelithiasis
disease
Digestive System Diseases
Disease or Syndrome
252
90
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
Bulla of lung
disease
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
Disease or Syndrome
11
2
0.010
None
1.000
1
1998
1998
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
Syphilis
disease
Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases
Disease or Syndrome
80
3
0.010
None
1.000
1
2003
2003
Malaria
disease
Infections
Disease or Syndrome
685
148
0.320
None
1.000
2
2001
2004
Yellow Fever
disease
Infections
Disease or Syndrome
28
0.010
None
1.000
1
2006
2006
Keratoconjunctivitis, Vernal
disease
Eye Diseases; Immune System Diseases
Disease or Syndrome
40
0.010
None
1.000
1
2007
2007
Atopic keratoconjunctivitis
disease
Eye Diseases; Immune System Diseases
Disease or Syndrome
9
0.010
None
1.000
1
2007
2007
Conjunctivitis, Giant Papillary
disease
Eye Diseases; Immune System Diseases
Disease or Syndrome
1
0.010
None
1.000
1
2007
2007