Spontaneous abortion
phenotype
Female Urogenital Diseases and Pregnancy Complications
Pathologic Function
188
0.100
None
0
Lipodystrophy
disease
Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
Disease or Syndrome
226
28
0.100
None
0
Oligohydramnios
phenotype
Female Urogenital Diseases and Pregnancy Complications
Pathologic Function
129
21
0.100
None
0
Premature Birth
phenotype
Female Urogenital Diseases and Pregnancy Complications
Pathologic Function
192
50
0.100
None
0
Increased antibody level in blood
phenotype
Finding
27
0.100
None
0
Small for gestational age (disorder)
phenotype
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications
Finding
181
34
0.100
None
0
Small for gestational age fetus
phenotype
Pathological Conditions, Signs and Symptoms
Finding
156
0.100
None
0
Facial edema
disease
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Male Urogenital Diseases; Immune System Diseases; Cardiovascular Diseases
Pathologic Function
9
1
0.100
None
0
Edema of foot (finding)
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
19
0.100
None
0
Increased alpha-globulin
phenotype
Finding
1
0.100
None
0
Recurrent lower respiratory tract infection
phenotype
Disease or Syndrome
23
0.100
None
0
ALBUMIN BLENHEIM PHENOTYPE
phenotype
Finding
1
1
0.100
None
0
1
Mild global developmental delay
phenotype
Finding
36
13
0.100
None
0
ALBUMIN B PHENOTYPE
phenotype
Finding
1
1
0.100
None
0
1
ANALBUMINEMIA BAGHDAD
phenotype
Finding
1
1
0.100
None
0
1
Low pulse pressure
phenotype
Finding
1
0.100
None
0
EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases
Disease or Syndrome
3
16
0.100
None
0
1
Aseptic Meningitis
disease
Nervous System Diseases
Disease or Syndrome
17
0.300
None
1.000
3
1970
1971
×
CUI:
C0030193
Disease:
Pain
Pain
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
1554
196
0.340
None
0.600
5
1973
2019
Myopathy
group
Musculoskeletal Diseases; Nervous System Diseases
Disease or Syndrome
634
166
0.300
None
1.000
1
1973
1973
X-linked agammaglobulinemia
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
Disease or Syndrome
68
69
0.010
None
1.000
1
1973
1973
Pain, Burning
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
56
0.300
None
1.000
1
1973
1973
×
CUI:
C0234238
Disease:
Ache
Ache
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
50
0.300
None
1.000
1
1973
1973
Radiating pain
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
51
0.300
None
1.000
1
1973
1973
Pain, Splitting
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
50
0.300
None
1.000
1
1973
1973