Maculopapular Lesion
phenotype
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Immune System Diseases
Finding
16
28
0.100
None
0
Increased mean corpuscular hemoglobin concentration
phenotype
Finding
13
0.100
None
0
Postnatal growth retardation
phenotype
Finding
121
11
0.100
None
0
Growth delay
phenotype
Pathologic Function
244
40
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
Hypofibrinogenemia
disease
Disease or Syndrome
60
14
0.100
None
0
Spherocytosis
phenotype
Finding
5
0.100
None
0
Stomatocytosis Result
phenotype
Laboratory or Test Result
13
0.100
None
0
Increased red cell osmotic fragility
phenotype
Finding
9
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
Frontal bossing
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Congenital Abnormality
321
22
0.100
None
0
Hepatomegaly
phenotype
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
Finding
523
30
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
Extramedullary Hematopoiesis Function
phenotype
Organ or Tissue Function
16
0.100
None
0
×
CUI:
C0018099
Disease:
Gout
Gout
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Disease or Syndrome
205
2354
0.100
None
0
×
CUI:
C0015967
Disease:
Fever
Fever
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
1021
66
0.100
None
0
Fatigue
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
760
67
0.100
None
0
1
Cholelithiasis
disease
Digestive System Diseases
Disease or Syndrome
252
90
0.100
None
0
Restrictive cardiomyopathy
disease
Cardiovascular Diseases
Disease or Syndrome
41
30
0.100
None
0
Ataxia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
868
68
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
Abdominal Pain
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
302
18
0.100
None
0
Abdomen distended
phenotype
Digestive System Diseases
Finding
103
6
0.100
None
0
Hyperbilirubinemia
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
131
27
0.100
None
0
Splenomegaly
phenotype
Pathological Conditions, Signs and Symptoms
Finding
345
19
0.100
None
0
1