Blackout - symptom
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases
|
Sign or Symptom
|
4
|
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Alcoholic blackout
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
|
Mental or Behavioral Dysfunction
|
4
|
|
0.010 |
None |
1.000 |
1 |
|
2013 |
2013 |
Congenital premature fusion
|
disease |
|
Congenital Abnormality
|
6
|
1
|
0.010 |
None |
1.000 |
1 |
|
1999 |
1999 |
Synostotic Anterior Plagiocephaly
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
16
|
|
0.320 |
None |
1.000 |
3 |
|
1999 |
2018 |
Craniosynostosis, Type 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Disease or Syndrome
|
18
|
28
|
0.300 |
None |
1.000 |
1 |
|
2003 |
2003 |
Peripheral arthritis
|
disease |
Musculoskeletal Diseases
|
Disease or Syndrome
|
22
|
15
|
0.010 |
None |
1.000 |
1 |
1
|
2019 |
2019 |
Congenital abnormal Synostosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
25
|
7
|
0.010 |
None |
1.000 |
1 |
|
2002 |
2002 |
Synostotic Posterior Plagiocephaly
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Disease or Syndrome
|
25
|
|
0.300 |
None |
1.000 |
1 |
|
2003 |
2003 |
Metopic synostosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
28
|
5
|
0.300 |
None |
1.000 |
1 |
|
2003 |
2003 |
Acrocephaly
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
35
|
|
0.300 |
None |
1.000 |
1 |
|
2003 |
2003 |
Sagittal craniosynostosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
35
|
13
|
0.010 |
None |
1.000 |
1 |
|
2006 |
2006 |
Small Fiber Neuropathy
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
35
|
8
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |
Scaphycephaly
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
43
|
8
|
0.310 |
None |
1.000 |
2 |
|
2003 |
2006 |
Neoplasms, Neuroepithelial
|
group |
Neoplasms
|
Neoplastic Process
|
46
|
5
|
0.010 |
None |
1.000 |
1 |
|
2001 |
2001 |
Cleidocranial Dysplasia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Disease or Syndrome
|
52
|
22
|
0.010 |
None |
1.000 |
1 |
|
2020 |
2020 |
Trigonocephaly
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
52
|
7
|
0.300 |
None |
1.000 |
1 |
|
2003 |
2003 |
Spinal fusion
|
disease |
|
Anatomical Abnormality
|
67
|
2
|
0.020 |
None |
1.000 |
2 |
|
2015 |
2019 |
Childhood Embryonal Rhabdomyosarcoma
|
disease |
Neoplasms
|
Neoplastic Process
|
67
|
7
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Idiopathic hypogonadotropic hypogonadism
|
disease |
Endocrine System Diseases
|
Disease or Syndrome
|
82
|
66
|
0.030 |
None |
1.000 |
3 |
|
2018 |
2019 |
Embryonal Rhabdomyosarcoma
|
disease |
Neoplasms
|
Neoplastic Process
|
121
|
8
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Abnormality of the skeletal system
|
disease |
|
Anatomical Abnormality
|
148
|
18
|
0.010 |
None |
1.000 |
1 |
|
2020 |
2020 |
Skin callus
|
disease |
Skin and Connective Tissue Diseases
|
Acquired Abnormality
|
154
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Brachycephaly
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
186
|
20
|
0.300 |
None |
1.000 |
1 |
|
2003 |
2003 |
Central Serous Chorioretinopathy
|
disease |
Eye Diseases
|
Disease or Syndrome
|
211
|
10
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Familial multiple trichoepitheliomata
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases
|
Neoplastic Process
|
317
|
32
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |