Cessation of head growth
|
disease |
|
Anatomical Abnormality
|
6
|
|
0.100 |
None |
|
0 |
|
|
|
Macrocephaly
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Congenital Abnormality
|
367
|
10
|
0.100 |
None |
|
0 |
|
|
|
Childhood Ataxia with Central Nervous System Hypomyelinization
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
59
|
63
|
0.800 |
strong |
0.906 |
32 |
8
|
2001 |
2020 |
Vanishing white matter disease
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
14
|
4
|
0.100 |
None |
0.917 |
24 |
|
2003 |
2019 |
Leukodystrophy
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
190
|
27
|
0.100 |
None |
0.952 |
21 |
|
2004 |
2019 |
Neurodegenerative Disorders
|
group |
Nervous System Diseases
|
Disease or Syndrome
|
1515
|
85
|
0.090 |
None |
0.889 |
9 |
|
2004 |
2018 |
Leukoencephalopathy
|
group |
Nervous System Diseases
|
Disease or Syndrome
|
189
|
17
|
0.170 |
None |
1.000 |
7 |
|
2002 |
2019 |
OVARIOLEUKODYSTROPHY
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Nervous System Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
7
|
9
|
0.550 |
None |
1.000 |
6 |
|
2004 |
2008 |
Cerebellar Ataxia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Disease or Syndrome
|
441
|
120
|
0.040 |
None |
1.000 |
4 |
|
2004 |
2009 |
Multiple Sclerosis
|
disease |
Immune System Diseases; Nervous System Diseases
|
Disease or Syndrome
|
1800
|
1022
|
0.030 |
None |
0.667 |
3 |
|
2008 |
2017 |
Encephalopathies
|
group |
Nervous System Diseases
|
Disease or Syndrome
|
457
|
64
|
0.030 |
None |
1.000 |
3 |
|
2003 |
2004 |
nervous system disorder
|
group |
Nervous System Diseases
|
Disease or Syndrome
|
977
|
39
|
0.020 |
None |
1.000 |
2 |
|
2012 |
2015 |
Brain Diseases
|
group |
Nervous System Diseases
|
Disease or Syndrome
|
345
|
10
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |
Scleroderma
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
316
|
5
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Down Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
766
|
80
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Leishmaniasis
|
disease |
Infections; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
198
|
4
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Premature Menopause
|
disease |
Female Urogenital Diseases and Pregnancy Complications
|
Disease or Syndrome
|
299
|
90
|
0.110 |
None |
1.000 |
1 |
|
2004 |
2004 |
Parkinson Disease
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
2078
|
990
|
0.010 |
None |
1.000 |
1 |
|
2005 |
2005 |
Systemic Scleroderma
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
979
|
287
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Ovarian Failure, Premature
|
disease |
Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
|
Disease or Syndrome
|
333
|
115
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |
Lung Diseases, Interstitial
|
group |
Respiratory Tract Diseases
|
Disease or Syndrome
|
319
|
144
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Diffuse Scleroderma
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
56
|
5
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Complete Trisomy 21 Syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
669
|
77
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Optic Atrophy
|
disease |
Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
568
|
51
|
0.100 |
None |
|
0 |
|
|
|
Primary physiologic amenorrhea
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
129
|
10
|
0.100 |
None |
|
0 |
|
|
|