COHEN-GIBSON SYNDROME
|
disease |
|
Disease or Syndrome
|
2
|
5
|
0.610 |
strong |
1.000 |
6 |
5
|
2015 |
2019 |
Weaver syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
8
|
13
|
0.370 |
None |
1.000 |
7 |
|
2017 |
2019 |
Peripheral Nerve Sheath Neoplasm
|
disease |
Neoplasms; Nervous System Diseases
|
Neoplastic Process
|
22
|
|
0.300 |
None |
1.000 |
1 |
|
2014 |
2014 |
Nerve Sheath Tumors
|
group |
Neoplasms; Nervous System Diseases
|
Neoplastic Process
|
31
|
|
0.300 |
None |
1.000 |
1 |
|
2014 |
2014 |
Neurilemmoma
|
disease |
Neoplasms
|
Neoplastic Process
|
193
|
11
|
0.300 |
None |
1.000 |
1 |
|
2014 |
2014 |
Schwannomatosis, Plexiform
|
disease |
Neoplasms
|
Neoplastic Process
|
5
|
|
0.300 |
None |
1.000 |
1 |
|
2014 |
2014 |
Perineurioma
|
disease |
Neoplasms; Nervous System Diseases
|
Neoplastic Process
|
18
|
3
|
0.300 |
None |
1.000 |
1 |
|
2014 |
2014 |
Transient Ischemic Attack
|
disease |
Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
344
|
16
|
0.200 |
None |
1.000 |
1 |
|
2013 |
2013 |
Intellectual Disability
|
group |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
|
Mental or Behavioral Dysfunction
|
2165
|
159
|
0.130 |
None |
1.000 |
3 |
|
2019 |
2019 |
Cryptorchidism
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases
|
Congenital Abnormality
|
725
|
80
|
0.110 |
None |
1.000 |
1 |
|
2019 |
2019 |
Body Height
|
phenotype |
|
Organism Attribute
|
1903
|
3972
|
0.100 |
None |
1.000 |
1 |
1
|
2019 |
2019 |
Redundant skin
|
phenotype |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Pathologic Function
|
48
|
2
|
0.100 |
None |
|
0 |
|
|
|
Congenital Epicanthus
|
disease |
|
Congenital Abnormality
|
417
|
30
|
0.100 |
None |
|
0 |
|
|
|
Congenital Camptodactyly
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
123
|
10
|
0.100 |
None |
|
0 |
|
|
|
Long fingers
|
phenotype |
|
Finding
|
32
|
6
|
0.100 |
None |
|
0 |
|
|
|
Congenital exomphalos
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Congenital Abnormality
|
235
|
|
0.100 |
None |
|
0 |
|
|
|
Depressed nasal bridge
|
phenotype |
|
Finding
|
426
|
39
|
0.100 |
None |
|
0 |
|
|
|
Long foot
|
phenotype |
Musculoskeletal Diseases
|
Finding
|
19
|
3
|
0.100 |
None |
|
0 |
1
|
|
|
Gait abnormality
|
group |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
312
|
23
|
0.100 |
None |
|
0 |
|
|
|
Poor coordination
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
26
|
8
|
0.100 |
None |
|
0 |
1
|
|
|
Downward slant of palpebral fissure
|
phenotype |
|
Finding
|
391
|
49
|
0.100 |
None |
|
0 |
|
|
|
Thin nails
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Finding
|
10
|
1
|
0.100 |
None |
|
0 |
|
|
|
Fine hair
|
phenotype |
|
Finding
|
69
|
1
|
0.100 |
None |
|
0 |
|
|
|
Large hand
|
phenotype |
|
Finding
|
35
|
7
|
0.100 |
None |
|
0 |
1
|
|
|
Broad thumbs
|
phenotype |
|
Finding
|
67
|
11
|
0.100 |
None |
|
0 |
|
|
|