Abnormal blistering of the skin
phenotype
Finding
75
10
0.100
None
0
Memory Impairment, CTCAE 3.0
phenotype
Finding
109
2
0.100
None
0
Malabsorption, CTCAE
phenotype
Finding
175
0.100
None
0
Retinopathy, CTCAE
phenotype
Finding
108
0.100
None
0
Dwarfism
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
Congenital Abnormality
1261
77
0.100
None
0
Cerebral Ischemia
disease
Nervous System Diseases; Cardiovascular Diseases
Pathologic Function
120
2
0.100
None
0
Bone marrow hypercellularity
phenotype
Finding
26
0.100
None
0
Decreased proportion of CD4-positive T cells
phenotype
Immune System Diseases; Hemic and Lymphatic Diseases
Finding
19
0.100
None
0
Developmental regression
disease
Mental Disorders
Disease or Syndrome
333
80
0.100
None
0
hypopigmented skin patch
phenotype
Skin and Connective Tissue Diseases
Finding
123
2
0.100
None
0
Skin Papule
phenotype
Skin and Connective Tissue Diseases
Finding
74
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
Blindness
phenotype
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
Disease or Syndrome
393
34
0.100
None
0
Coombs positive hemolytic anemia
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
6
0.100
None
0
Gait abnormality
group
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
312
23
0.100
None
0
Mitral Valve Insufficiency
phenotype
Cardiovascular Diseases
Pathologic Function
94
11
0.100
None
0
Premature Menopause
disease
Female Urogenital Diseases and Pregnancy Complications
Disease or Syndrome
299
90
0.100
None
0
Irritable Mood
phenotype
Behavior and Behavior Mechanisms
Finding
142
1
0.100
None
0
Meningitis
disease
Nervous System Diseases
Disease or Syndrome
191
13
0.100
None
0
Keratoconjunctivitis Sicca
disease
Eye Diseases
Disease or Syndrome
90
3
0.100
None
0
×
CUI:
C0702166
Disease:
Acne
Acne
disease
Skin and Connective Tissue Diseases
Disease or Syndrome
167
11
0.100
None
0
Malabsorption Syndrome
group
Digestive System Diseases; Nutritional and Metabolic Diseases
Disease or Syndrome
239
0.100
None
0
Antineutrophil antibody positivity
phenotype
Laboratory or Test Result
15
0.100
None
0
Weight decreased
phenotype
Pathological Conditions, Signs and Symptoms
Finding
271
3
0.100
None
0
Myositis
disease
Musculoskeletal Diseases; Nervous System Diseases
Disease or Syndrome
254
43
0.100
None
0