Muscle fiber cytoplasmatic inclusion bodies
|
phenotype |
|
Finding
|
2
|
|
0.100 |
None |
|
0 |
|
|
|
Fatiguable weakness of proximal limb muscles
|
phenotype |
|
Finding
|
14
|
|
0.100 |
None |
|
0 |
|
|
|
Abnormal peripheral nervous system morphology
|
disease |
|
Anatomical Abnormality
|
4
|
2
|
0.100 |
None |
|
0 |
|
|
|
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 5
|
disease |
|
Disease or Syndrome
|
1
|
2
|
0.100 |
None |
|
0 |
2
|
|
|
Two-raphe bicuspid aortic valve
|
disease |
Cardiovascular Diseases
|
Congenital Abnormality
|
1
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Finger flexor weakness
|
phenotype |
|
Finding
|
2
|
|
0.100 |
None |
|
0 |
|
|
|
Abnormal morphology of left ventricular trabeculae
|
phenotype |
|
Anatomical Abnormality
|
1
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Abnormal ventricular septum morphology
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Anatomical Abnormality
|
2
|
1
|
0.100 |
None |
|
0 |
1
|
|
|
Intrinsic hand muscle atrophy
|
phenotype |
|
Finding
|
11
|
|
0.100 |
None |
|
0 |
|
|
|
Foramen Ovale, Patent
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
73
|
14
|
0.100 |
None |
|
0 |
1
|
|
|
Distal upper limb amyotrophy
|
disease |
|
Disease or Syndrome
|
8
|
1
|
0.100 |
None |
|
0 |
|
|
|
Dyspnea
|
phenotype |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
|
Sign or Symptom
|
222
|
26
|
0.100 |
None |
|
0 |
|
|
|
Decreased finger mobility
|
phenotype |
Musculoskeletal Diseases
|
Finding
|
1
|
|
0.100 |
None |
|
0 |
|
|
|
Proximal muscle weakness in lower limbs
|
phenotype |
|
Finding
|
30
|
4
|
0.100 |
None |
|
0 |
|
|
|
Foot dorsiflexor weakness
|
phenotype |
|
Finding
|
70
|
4
|
0.100 |
None |
|
0 |
|
|
|
Congestive heart failure
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
1760
|
165
|
0.100 |
None |
|
0 |
|
|
|
Distal upper limb muscle weakness
|
phenotype |
|
Finding
|
13
|
3
|
0.100 |
None |
|
0 |
|
|
|
Hip flexor weakness
|
phenotype |
|
Finding
|
16
|
1
|
0.100 |
None |
|
0 |
|
|
|
Lymphoma, Diffuse
|
disease |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
|
Neoplastic Process
|
49
|
|
0.010 |
None |
1.000 |
1 |
|
1983 |
1983 |
Plasmacytoma
|
disease |
Neoplasms; Immune System Diseases
|
Neoplastic Process
|
142
|
8
|
0.010 |
None |
1.000 |
1 |
|
1983 |
1983 |
Muscular Dystrophy, Emery-Dreifuss
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
44
|
18
|
0.010 |
None |
1.000 |
1 |
|
1993 |
1993 |
Muscular Dystrophies, Limb-Girdle
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
118
|
37
|
0.020 |
None |
1.000 |
2 |
|
2000 |
2003 |
Eosinophilic disorder
|
group |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
288
|
22
|
0.010 |
None |
1.000 |
1 |
|
2005 |
2005 |
Eosinophilia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
325
|
23
|
0.010 |
None |
1.000 |
1 |
|
2005 |
2005 |
Allergic rhinitis (disorder)
|
disease |
Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases
|
Disease or Syndrome
|
446
|
176
|
0.010 |
None |
1.000 |
1 |
|
2006 |
2006 |