Aneurysm of femoral artery
|
phenotype |
|
Anatomical Abnormality
|
1
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Patellar subluxation
|
phenotype |
|
Pathologic Function
|
2
|
|
0.100 |
None |
|
0 |
|
|
|
Abnormally folded helix
|
phenotype |
|
Finding
|
2
|
|
0.100 |
None |
|
0 |
|
|
|
Calf muscle hypoplasia
|
phenotype |
|
Finding
|
2
|
|
0.100 |
None |
|
0 |
|
|
|
ARTHROGRYPOSIS, DISTAL, TYPE 4 (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Disease or Syndrome
|
3
|
|
0.200 |
None |
1.000 |
3 |
|
2001 |
2010 |
Arthrogryposis, distal, type 2E
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Disease or Syndrome
|
3
|
|
0.200 |
None |
1.000 |
3 |
|
2001 |
2010 |
ARTHROGRYPOSIS, DISTAL, TYPE 10
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Disease or Syndrome
|
3
|
|
0.200 |
None |
1.000 |
3 |
|
2001 |
2010 |
Arthrogryposis-like hand anomaly and sensorineural deafness
|
phenotype |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
|
Disease or Syndrome
|
3
|
|
0.200 |
None |
1.000 |
3 |
|
2001 |
2010 |
Distal arthrogryposis type 5D
|
disease |
|
Disease or Syndrome
|
3
|
20
|
0.200 |
None |
1.000 |
3 |
|
2001 |
2010 |
Neonatal Marfan syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
3
|
8
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
Oculomelic amyoplasia
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
4
|
11
|
0.200 |
None |
1.000 |
3 |
|
2001 |
2010 |
ARTHROGRYPOSIS, DISTAL, TYPE 1B
|
disease |
|
Disease or Syndrome
|
4
|
3
|
0.200 |
None |
1.000 |
3 |
|
2001 |
2010 |
Opisthorchis viverrini Infection
|
disease |
Infections
|
Disease or Syndrome
|
4
|
|
0.010 |
None |
1.000 |
1 |
|
2011 |
2011 |
Flexion contracture of hip
|
disease |
Musculoskeletal Diseases
|
Acquired Abnormality
|
4
|
5
|
0.100 |
None |
|
0 |
1
|
|
|
Abnormality of connective tissue
|
disease |
|
Anatomical Abnormality
|
4
|
3
|
0.100 |
None |
|
0 |
1
|
|
|
Hecht syndrome (disorder)
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
5
|
1
|
0.200 |
None |
1.000 |
3 |
|
2001 |
2010 |
MACULAR DEGENERATION, EARLY-ONSET
|
disease |
|
Disease or Syndrome
|
6
|
3
|
0.500 |
None |
1.000 |
1 |
2
|
2014 |
2014 |
Crumpled ear
|
disease |
|
Finding
|
6
|
5
|
0.100 |
None |
|
0 |
1
|
|
|
Intestinal schistosomiasis
|
disease |
Infections
|
Disease or Syndrome
|
8
|
|
0.020 |
None |
1.000 |
2 |
|
2017 |
2017 |
ARTHROGRYPOSIS, DISTAL, TYPE 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Disease or Syndrome; Congenital Abnormality
|
9
|
10
|
0.200 |
None |
1.000 |
3 |
|
2001 |
2010 |
Hereditary Connective Tissue Disorder
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
9
|
|
0.020 |
None |
1.000 |
2 |
|
1983 |
1999 |
Hereditary sideroblastic anemia
|
disease |
Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
9
|
1
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Camptodactyly of toe
|
disease |
|
Anatomical Abnormality
|
9
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Visceral Myopathy
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
10
|
19
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Recurrent Hepatocellular Carcinoma
|
disease |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
12
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |