TENORIO SYNDROME
disease
Disease or Syndrome
1
3
0.700
strong
1.000
1
3
2014
2014
Large forehead
phenotype
Finding
14
1
0.100
None
0
Persistent cavum septum pellucidum
phenotype
Finding
17
2
0.100
None
0
Congenital hemihypertrophy
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications
Congenital Abnormality
23
2
0.100
None
0
Overgrowth Syndrome
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
36
6
0.010
None
1.000
1
2014
2014
Hypoinsulinaemia (disorder)
disease
Disease or Syndrome
36
0.100
None
0
Late fontanel closure
phenotype
Finding
41
0.100
None
0
Clumsiness
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders
Sign or Symptom
48
3
0.100
None
0
Raynaud Phenomenon
disease
Cardiovascular Diseases
Disease or Syndrome
63
1
0.100
None
0
Wide nose
phenotype
Finding
87
1
0.100
None
0
Keratoconjunctivitis Sicca
disease
Eye Diseases
Disease or Syndrome
90
3
0.100
None
0
Hypertrichosis
disease
Skin and Connective Tissue Diseases
Disease or Syndrome
92
27
0.100
None
0
Motor retardation
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms
Finding
98
8
0.100
None
0
Thick eyebrow
phenotype
Finding
104
13
0.100
None
0
Stomatitis
disease
Stomatognathic Diseases
Disease or Syndrome
109
22
0.100
None
0
Macroglossia
disease
Stomatognathic Diseases
Disease or Syndrome
115
2
0.100
None
0
Japanese Encephalitis
disease
Infections; Nervous System Diseases
Disease or Syndrome
119
6
0.010
None
1.000
1
2015
2015
Syncope
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
119
45
0.100
None
0
Telecanthus
phenotype
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Finding
134
14
0.100
None
0
Class III malocclusion
disease
Stomatognathic Diseases
Congenital Abnormality
181
19
0.100
None
0
Cerebral Palsy
disease
Nervous System Diseases
Disease or Syndrome
241
69
0.100
None
0
×
CUI:
C0003578
Disease:
Apnea
Apnea
phenotype
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
Sign or Symptom
262
11
0.100
None
0
Cerebral cortical atrophy
disease
Disease or Syndrome
271
13
0.100
None
0
Gait Disturbance, CTCAE
phenotype
Finding
299
0.100
None
0
Gait abnormality
group
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
312
23
0.100
None
0