Precursor Cell Lymphoblastic Leukemia Lymphoma
|
disease |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
|
Neoplastic Process
|
1
|
1
|
0.400 |
None |
|
0 |
1
|
|
|
Congenital Hypothyroidism
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
6
|
9
|
0.100 |
None |
|
0 |
1
|
|
|
Generalized hypotonia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
128
|
164
|
0.100 |
None |
|
0 |
1
|
|
|
Delayed speech and language development
|
phenotype |
Behavior and Behavior Mechanisms
|
Finding
|
124
|
192
|
0.100 |
None |
|
0 |
1
|
|
|
Uranostaphyloschisis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases
|
Congenital Abnormality
|
21
|
24
|
0.100 |
None |
|
0 |
2
|
|
|
MYELODYSPLASTIC SYNDROME
|
group |
Hemic and Lymphatic Diseases
|
Neoplastic Process
|
11
|
19
|
0.100 |
None |
|
0 |
1
|
|
|
Infantile axial hypotonia
|
phenotype |
|
Finding
|
7
|
8
|
0.100 |
None |
|
0 |
1
|
|
|
Upper limb hypertonia
|
phenotype |
|
Anatomical Abnormality
|
4
|
4
|
0.100 |
None |
|
0 |
1
|
|
|
Neurodevelopmental abnormality
|
phenotype |
|
Pathologic Function
|
6
|
19
|
0.100 |
None |
|
0 |
1
|
|
|
Neurodevelopmental delay
|
phenotype |
|
Finding
|
17
|
24
|
0.100 |
None |
|
0 |
1
|
|
|
Acute lymphocytic leukemia
|
disease |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
|
Neoplastic Process
|
5
|
12
|
0.100 |
None |
|
0 |
2
|
|
|
Hypothyroidism
|
disease |
Endocrine System Diseases
|
Disease or Syndrome
|
25
|
28
|
0.100 |
None |
|
0 |
1
|
|
|
Esotropia
|
disease |
Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
33
|
38
|
0.100 |
None |
|
0 |
1
|
|
|
Dystonia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
42
|
61
|
0.100 |
None |
|
0 |
2
|
|
|
Dystonia, Limb
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
6
|
8
|
0.100 |
None |
|
0 |
1
|
|
|
MENTAL RETARDATION, AUTOSOMAL DOMINANT 42
|
disease |
|
Disease or Syndrome
|
1
|
6
|
0.700 |
None |
1.000 |
1 |
6
|
2015 |
2018 |
Global developmental delay
|
disease |
|
Mental or Behavioral Dysfunction
|
303
|
505
|
0.420 |
strong |
1.000 |
1 |
9
|
2016 |
2019 |
Seizures
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
237
|
417
|
0.410 |
strong |
1.000 |
1 |
8
|
2015 |
2016 |
Cortical visual impairment
|
phenotype |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Pathologic Function
|
21
|
27
|
0.100 |
None |
1.000 |
1 |
2
|
2016 |
2016 |
EEG with generalized epileptiform discharges
|
phenotype |
|
Finding
|
2
|
4
|
0.100 |
None |
1.000 |
1 |
3
|
2016 |
2016 |
Nystagmus
|
disease |
Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
62
|
83
|
0.100 |
None |
1.000 |
1 |
2
|
2016 |
2016 |
Multifocal epileptiform discharges
|
phenotype |
|
Finding
|
7
|
9
|
0.100 |
None |
1.000 |
1 |
3
|
2016 |
2016 |
Strabismus
|
disease |
Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
61
|
85
|
0.100 |
None |
1.000 |
1 |
4
|
2016 |
2016 |
Feeding difficulties
|
phenotype |
|
Finding
|
45
|
62
|
0.100 |
None |
1.000 |
1 |
3
|
2016 |
2016 |
Complex partial seizure with impairment of consciousness
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Disease or Syndrome
|
7
|
10
|
0.100 |
None |
1.000 |
1 |
3
|
2016 |
2016 |