Hyperglycinemia, Transient Neonatal
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
2
|
|
0.010 |
None |
1.000 |
1 |
|
2002 |
2002 |
Aggressive outburst
|
disease |
Behavior and Behavior Mechanisms
|
Mental or Behavioral Dysfunction
|
2
|
2
|
0.010 |
None |
1.000 |
1 |
2
|
2005 |
2005 |
Hyperglycinemia, Nonketotic, Type I
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
3
|
|
0.300 |
None |
1.000 |
3 |
|
2006 |
2007 |
Hyperglycinemia, Nonketotic, Type II
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
3
|
|
0.300 |
None |
1.000 |
3 |
|
2006 |
2007 |
Hyperglycinemia, Nonketotic, Type III
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
3
|
|
0.300 |
None |
1.000 |
3 |
|
2006 |
2007 |
Psychotic behaviour
|
disease |
|
Mental or Behavioral Dysfunction
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
2015 |
2015 |
Recurrent singultus
|
phenotype |
|
Finding
|
3
|
|
0.100 |
None |
|
0 |
|
|
|
Chromosome 9, partial trisomy 9p
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
4
|
|
0.010 |
None |
1.000 |
1 |
|
1989 |
1989 |
CHROMOSOME 9p DELETION SYNDROME
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
5
|
|
0.010 |
None |
1.000 |
1 |
|
1989 |
1989 |
Hyperglycinemia
|
phenotype |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
14
|
|
0.100 |
None |
|
0 |
|
|
|
HYPERGLYCINURIA (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Disease or Syndrome
|
14
|
3
|
0.100 |
None |
|
0 |
|
|
|
Nonketotic Hyperglycinemia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
21
|
182
|
1.000 |
definitive |
0.982 |
56 |
136
|
1990 |
2020 |
Psychomotor Agitation
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms
|
Finding
|
26
|
|
0.100 |
None |
|
0 |
|
|
|
Glycine measurement
|
phenotype |
|
Laboratory Procedure
|
32
|
68
|
0.100 |
None |
1.000 |
1 |
2
|
2019 |
2019 |
Conduct Disorder
|
disease |
Mental Disorders
|
Mental or Behavioral Dysfunction
|
34
|
18
|
0.010 |
None |
1.000 |
1 |
|
2015 |
2015 |
Carcinoma, Large Cell
|
disease |
Neoplasms
|
Neoplastic Process
|
90
|
6
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Deuteranomaly
|
disease |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
92
|
10
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Epilepsy, Generalized
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
93
|
36
|
0.100 |
None |
1.000 |
1 |
1
|
2000 |
2000 |
Choreoathetosis
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Disease or Syndrome
|
94
|
9
|
0.010 |
None |
1.000 |
1 |
1
|
2011 |
2011 |
Russell-Silver syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Disease or Syndrome
|
104
|
12
|
0.010 |
None |
1.000 |
1 |
|
2010 |
2010 |
Abnormality of brain morphology
|
phenotype |
|
Anatomical Abnormality
|
104
|
131
|
0.100 |
None |
|
0 |
1
|
|
|
stage, non-small cell lung cancer
|
disease |
Neoplasms; Respiratory Tract Diseases
|
Neoplastic Process
|
107
|
6
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Irritability, CTCAE
|
phenotype |
|
Finding
|
140
|
|
0.100 |
None |
|
0 |
|
|
|
Irritable Mood
|
phenotype |
Behavior and Behavior Mechanisms
|
Finding
|
142
|
1
|
0.100 |
None |
|
0 |
|
|
|
Death in infancy
|
phenotype |
|
Finding
|
146
|
7
|
0.100 |
None |
|
0 |
|
|
|