CARDIOMYOPATHY, DILATED, 1O
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
7
|
0.700 |
None |
1.000 |
9 |
7
|
2004 |
2017 |
ATRIAL FIBRILLATION, FAMILIAL, 12
|
disease |
|
Disease or Syndrome
|
1
|
2
|
0.700 |
None |
1.000 |
5 |
2
|
2004 |
2017 |
Acromegaloid facial appearance syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases
|
Disease or Syndrome
|
1
|
|
0.300 |
None |
1.000 |
1 |
|
2013 |
2013 |
Widened posterior fossa
|
phenotype |
|
Finding
|
1
|
|
0.100 |
None |
|
0 |
|
|
|
Congenital hypertrophy of left ventricle
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Congenital Abnormality
|
1
|
|
0.100 |
None |
|
0 |
|
|
|
Hypoplastic ischiopubic rami
|
phenotype |
|
Finding
|
1
|
|
0.100 |
None |
|
0 |
|
|
|
Cuboid-shaped vertebral bodies
|
phenotype |
|
Finding
|
2
|
|
0.100 |
None |
|
0 |
|
|
|
Impaired myocardial contractility
|
disease |
|
Disease or Syndrome
|
2
|
|
0.100 |
None |
|
0 |
|
|
|
Prinzmetal's variant angina
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
3
|
|
0.010 |
None |
1.000 |
1 |
|
2002 |
2002 |
Large sella turcica
|
phenotype |
|
Finding
|
3
|
|
0.100 |
None |
|
0 |
|
|
|
Oral synechia
|
phenotype |
|
Finding
|
3
|
|
0.100 |
None |
|
0 |
|
|
|
Cantu syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
4
|
14
|
0.800 |
definitive |
0.950 |
20 |
12
|
1996 |
2020 |
Broad first metatarsal
|
phenotype |
|
Finding
|
4
|
1
|
0.100 |
None |
|
0 |
|
|
|
Congenital hypertrichosis lanuginosa
|
disease |
Skin and Connective Tissue Diseases
|
Congenital Abnormality
|
6
|
|
0.010 |
None |
1.000 |
1 |
|
2015 |
2015 |
Congenital hypertrichosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases
|
Congenital Abnormality
|
6
|
|
0.010 |
None |
1.000 |
1 |
|
2015 |
2015 |
Erlenmeyer flask deformity of the femurs
|
phenotype |
|
Finding
|
7
|
|
0.100 |
None |
|
0 |
|
|
|
Arteriolosclerosis
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
13
|
2
|
0.020 |
None |
1.000 |
2 |
1
|
2016 |
2017 |
Shortened QT interval
|
phenotype |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Finding
|
13
|
|
0.300 |
limited |
1.000 |
1 |
|
2005 |
2005 |
Curly eyelashes
|
phenotype |
|
Finding
|
15
|
|
0.100 |
None |
|
0 |
|
|
|
Thick upper lip vermilion
|
phenotype |
|
Finding
|
16
|
4
|
0.100 |
None |
|
0 |
|
|
|
Thick nasal alae
|
phenotype |
|
Finding
|
17
|
|
0.100 |
None |
|
0 |
|
|
|
Broad hallux phalanx
|
disease |
|
Anatomical Abnormality
|
17
|
|
0.100 |
None |
|
0 |
|
|
|
Broad ribs
|
phenotype |
|
Finding
|
18
|
|
0.100 |
None |
|
0 |
|
|
|
Deep plantar creases
|
phenotype |
|
Finding
|
19
|
6
|
0.100 |
None |
|
0 |
|
|
|
ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
22
|
1
|
0.300 |
None |
1.000 |
1 |
|
2007 |
2007 |