TTN-AS1, TTN antisense RNA 1, 100506866

N. diseases: 112; N. variants: 626
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
phenotype Neoplastic Process 6626 169 0.030 None 1.000 3 2019 2020
CUI: C0042834
Disease: Vital capacity
Vital capacity
phenotype Clinical Attribute 430 746 0.100 None 1.000 1 1 2019 2019
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval
phenotype Finding 57 138 0.100 None 1.000 1 1 2018 2018
Malignant neoplasm of colon and/or rectum
disease Neoplastic Process 3669 502 0.010 None 1.000 1 2020 2020
CUI: C0234182
Disease: Gowers sign
Gowers sign
phenotype Finding 54 8 0.100 None 0 1
Re-entrant atrioventricular tachycardia
disease Disease or Syndrome 2 2 0.100 None 0 2
CUI: C0423112
Disease: Short palpebral fissure
Short palpebral fissure
phenotype Finding 91 16 0.100 None 0 1
CUI: C0427063
Disease: Shoulder girdle weakness
Shoulder girdle weakness
phenotype Finding 39 4 0.100 None 0 2
CUI: C0856863
Disease: Broad-based gait
Broad-based gait
phenotype Finding 75 24 0.100 None 0 1
CUI: C1321329
Disease: Slowed saccades
Slowed saccades
phenotype Finding 29 4 0.100 None 0 2
CUI: C1836118
Disease: LEFT VENTRICULAR NONCOMPACTION 2
LEFT VENTRICULAR NONCOMPACTION 2
disease Disease or Syndrome 2 1 0.100 None 0 1
CUI: C1836150
Disease: Gait imbalance
Gait imbalance
phenotype Finding 57 24 0.100 None 0 2
CUI: C1836767
Disease: Proximal lower limb amyotrophy
Proximal lower limb amyotrophy
phenotype Finding 15 4 0.100 None 0 2
CUI: C1837108
Disease: Decreased muscle mass
Decreased muscle mass
phenotype Finding 65 12 0.100 None 0 2
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide
phenotype Finding 429 29 0.100 None 0 1
CUI: C1853932
Disease: Rimmed vacuoles on biopsy
Rimmed vacuoles on biopsy
phenotype Finding 28 2 0.100 None 0 1
CUI: C1856872
Disease: Down-sloping shoulders
Down-sloping shoulders
phenotype Finding 32 4 0.100 None 0 2
CUI: C1858033
Disease: Asymmetry of the thorax
Asymmetry of the thorax
phenotype Finding 12 4 0.100 None 0 2
CUI: C3277184
Disease: Decreased patellar reflex
Decreased patellar reflex
phenotype Finding 8 2 0.100 None 0 2
CUI: C3277226
Disease: Restrictive ventilatory defect
Restrictive ventilatory defect
phenotype Finding 61 8 0.100 None 0 2
CUI: C3805969
Disease: Scapular muscle atrophy
Scapular muscle atrophy
phenotype Finding 4 2 0.100 None 0 2
CUI: C4021054
Disease: Reduced muscle collagen VI
Reduced muscle collagen VI
phenotype Finding 5 2 0.100 None 0 2
Morphological abnormality of the central nervous system
group Anatomical Abnormality 10 7 0.100 None 0 1
CUI: C4021803
Disease: Abnormal eyelid morphology
Abnormal eyelid morphology
disease Anatomical Abnormality 10 3 0.100 None 0 2
CUI: C4023223
Disease: Atrial reentry tachycardia
Atrial reentry tachycardia
phenotype Pathologic Function 2 2 0.100 None 0 2