LBR, lamin B receptor, 3930

N. diseases: 307; N. variants: 17
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: C1839731
Disease: 11 pairs of ribs
11 pairs of ribs
phenotype Finding 20 3 0.100 None 0
CUI: C3266843
Disease: 47, XYY syndrome
47, XYY syndrome
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 9 0.030 None 1.000 3 1984 1997
CUI: C4021241
Disease: Abnormal foot bone ossification
Abnormal foot bone ossification
disease Musculoskeletal Diseases Anatomical Abnormality 3 0.100 None 0
CUI: C0240083
Disease: Abnormal joint morphology
Abnormal joint morphology
phenotype Musculoskeletal Diseases Finding 6 0.100 None 0
CUI: C0685695
Disease: Abnormal lung lobation
Abnormal lung lobation
disease Respiratory Tract Diseases Congenital Abnormality 32 0.100 None 0
Abnormal ossification involving the femoral head and neck
phenotype Finding 3 0.100 None 0
CUI: C4021525
Disease: Abnormal pelvis bone ossification
Abnormal pelvis bone ossification
disease Anatomical Abnormality 7 0.100 None 0
Abnormality of chromosome segregation
phenotype Finding 5 0.100 None 0
CUI: C4024689
Disease: Abnormality of the calcaneus
Abnormality of the calcaneus
disease Anatomical Abnormality 2 0.100 None 0
CUI: C0262444
Disease: Abnormality of the dentition
Abnormality of the dentition
phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases Finding 140 16 0.100 None 0
CUI: C4025362
Disease: Abnormality of the gastric mucosa
Abnormality of the gastric mucosa
disease Anatomical Abnormality 12 0.100 None 0
CUI: C4025863
Disease: Abnormality of the orbital region
Abnormality of the orbital region
phenotype Anatomical Abnormality 5 0.100 None 0
CUI: C4025828
Disease: Abnormality of the scapula
Abnormality of the scapula
disease Anatomical Abnormality 3 0.100 None 0
Abnormality of the vertebral spinous processes
disease Anatomical Abnormality 2 1 0.100 None 0
CUI: C4020966
Disease: Abnormally ossified vertebrae
Abnormally ossified vertebrae
disease Anatomical Abnormality 8 0.100 None 0
Absent or minimally ossified vertebral bodies
phenotype Finding 9 0.100 None 0
CUI: C1844555
Disease: Absent toenail
Absent toenail
phenotype Pathological Conditions, Signs and Symptoms Congenital Abnormality 11 0.100 None 0
CUI: C0022602
Disease: Actinic keratosis
Actinic keratosis
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 136 10 0.010 None 1.000 1 1983 1983
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
disease Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 639 50 0.010 None 1.000 1 1987 1987
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 1293 222 0.010 None 1.000 1 1985 1985
CUI: C0023487
Disease: Acute Promyelocytic Leukemia
Acute Promyelocytic Leukemia
disease Neoplasms Neoplastic Process 651 21 0.010 None 1.000 1 1988 1988
CUI: C0001361
Disease: Acute tonsillitis
Acute tonsillitis
disease Infections; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 2 1 0.010 None 1.000 1 2007 2007
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma
group Neoplasms Neoplastic Process 2235 168 0.010 None 1.000 1 1981 1981
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia
disease Neoplastic Process 860 154 0.010 None 1.000 1 1985 1985
CUI: C0278608
Disease: Adult Liposarcoma
Adult Liposarcoma
disease Neoplasms Neoplastic Process 143 6 0.010 None 1.000 1 1988 1988