Diarrhea
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
632
|
63
|
0.100 |
None |
|
0 |
|
|
|
Chronic oral candidiasis
|
disease |
Infections; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
8
|
2
|
0.100 |
None |
|
0 |
2
|
|
|
Severe T-cell immunodeficiency
|
disease |
|
Disease or Syndrome
|
5
|
2
|
0.100 |
None |
|
0 |
1
|
|
|
Medial calcification of large arteries
|
phenotype |
|
Pathologic Function
|
2
|
1
|
0.100 |
None |
|
0 |
|
|
|
Hypertension, Renovascular
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
78
|
8
|
0.100 |
None |
|
0 |
|
|
|
Immune dysregulation
|
phenotype |
|
Finding
|
11
|
1
|
0.100 |
None |
|
0 |
|
|
|
Short Stature, CTCAE
|
phenotype |
|
Finding
|
1010
|
|
0.100 |
None |
|
0 |
|
|
|
Recurrent Staphylococcus aureus infections
|
phenotype |
|
Finding
|
11
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Abnormal serum interferon-gamma level
|
phenotype |
|
Finding
|
2
|
|
0.100 |
None |
|
0 |
|
|
|
Pediatric failure to thrive
|
disease |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Mental Disorders
|
Disease or Syndrome
|
166
|
122
|
0.100 |
None |
|
0 |
1
|
|
|
Delayed speech and language development
|
phenotype |
Behavior and Behavior Mechanisms
|
Finding
|
560
|
192
|
0.100 |
None |
|
0 |
1
|
|
|
Chronic diarrhea
|
disease |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
|
Disease or Syndrome
|
62
|
9
|
0.100 |
None |
|
0 |
1
|
|
|
Primary Hypothyroidism
|
disease |
Endocrine System Diseases
|
Disease or Syndrome
|
19
|
3
|
0.100 |
None |
|
0 |
1
|
|
|
Villous atrophy
|
phenotype |
|
Finding
|
19
|
|
0.100 |
None |
|
0 |
|
|
|
Thyroiditis
|
disease |
Endocrine System Diseases
|
Disease or Syndrome
|
104
|
7
|
0.100 |
None |
|
0 |
|
|
|
Enterocolitis
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
40
|
2
|
0.100 |
None |
|
0 |
|
|
|
Functional abnormality of the bladder
|
phenotype |
|
Finding
|
3
|
|
0.100 |
None |
|
0 |
|
|
|
Idiopathic pulmonary arterial hypertension
|
disease |
Respiratory Tract Diseases
|
Disease or Syndrome
|
776
|
24
|
0.100 |
None |
|
0 |
|
|
|
Foramen Ovale, Patent
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
73
|
14
|
0.100 |
None |
|
0 |
|
|
|
Pulmonary arterial hypertension
|
disease |
Respiratory Tract Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
413
|
70
|
0.100 |
None |
|
0 |
|
|
|
Congestive heart failure
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
1760
|
165
|
0.100 |
None |
|
0 |
|
|
|
Onychomycosis
|
disease |
Infections; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
27
|
2
|
0.100 |
None |
|
0 |
1
|
|
|
Antiphospholipid antibody positivity
|
phenotype |
|
Finding
|
18
|
|
0.100 |
None |
|
0 |
|
|
|
Recurrent Aspergillus infections
|
phenotype |
|
Finding
|
5
|
|
0.100 |
None |
|
0 |
|
|
|
Recurrent mycobacterial infections
|
phenotype |
|
Finding
|
9
|
|
0.100 |
None |
|
0 |
|
|
|