Abdomen distended
phenotype
Digestive System Diseases
Finding
103
6
0.100
None
0
Extramedullary Hematopoiesis Function
phenotype
Organ or Tissue Function
16
0.100
None
0
Growth delay
phenotype
Pathologic Function
244
40
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
Elliptocytosis found
phenotype
Finding
12
0.100
None
0
Thrombophilia
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
161
43
0.100
None
0
stomatocytic anemia
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
15
1
0.100
None
0
Myalgia
phenotype
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
Sign or Symptom
226
22
0.100
None
0
Frontal bossing
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Congenital Abnormality
321
22
0.100
None
0
Reticulocytosis
phenotype
Pathological Conditions, Signs and Symptoms
Finding
40
1
0.100
None
0
Maculopapular Lesion
phenotype
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Immune System Diseases
Finding
16
28
0.100
None
0
Pallor
phenotype
Pathological Conditions, Signs and Symptoms
Finding
124
4
0.100
None
0
Skin Ulcer
phenotype
Skin and Connective Tissue Diseases
Disease or Syndrome
151
1
0.100
None
0
Muscle Weakness
phenotype
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
Sign or Symptom
536
87
0.100
None
0
Splenomegaly
phenotype
Pathological Conditions, Signs and Symptoms
Finding
345
19
0.100
None
0
Hypofibrinogenemia
disease
Disease or Syndrome
60
14
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
Spherocytosis
phenotype
Finding
5
0.100
None
0
Abdominal Pain
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
302
18
0.100
None
0
Increased mean corpuscular hemoglobin concentration
phenotype
Finding
13
0.100
None
0
Fibrinogen Deficiency
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Disease or Syndrome
56
4
0.100
None
0
Microspherocytosis
disease
Disease or Syndrome
13
1
0.100
None
0
Spontaneous hemolytic crises
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
7
0.100
None
0
Ataxia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
868
68
0.100
None
0