CD2AP, CD2 associated protein, 23607

N. diseases: 113; N. variants: 14
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: C1842982
Disease: FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3, SUSCEPTIBILITY TO
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3, SUSCEPTIBILITY TO 		phenotype Finding 1 1 0.400 None 1.000 2 1 2007 2019
CUI: C0859023
Disease: Talkativeness
Talkativeness 		disease Mental or Behavioral Dysfunction 1 0.010 None 1.000 1 2013 2013
CUI: C4016880
Disease: FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3 		disease Finding 1 2 0.100 None 0 2
CUI: C0020732
Disease: Iatrogenic Disease
Iatrogenic Disease 		group Pathological Conditions, Signs and Symptoms Disease or Syndrome 2 0.020 None 1.000 2 2017 2019
CUI: C3887755
Disease: Mountain Sickness
Mountain Sickness 		disease Respiratory Tract Diseases Disease or Syndrome 3 0.010 None 1.000 1 2012 2012
CUI: C3711850
Disease: Opticospinal Multiple Sclerosis
Opticospinal Multiple Sclerosis 		disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 7 0.010 None 1.000 1 2007 2007
CUI: C0002351
Disease: Altitude Sickness
Altitude Sickness 		phenotype Respiratory Tract Diseases Disease or Syndrome 10 0.010 None 1.000 1 2012 2012
CUI: C0549225
Disease: Myasthenic Syndrome
Myasthenic Syndrome 		disease Disease or Syndrome 12 0.010 None 1.000 1 2018 2018
CUI: C1868717
Disease: Behavioural and psychiatric symptoms of dementia
Behavioural and psychiatric symptoms of dementia 		disease Mental or Behavioral Dysfunction 14 2 0.010 None 1.000 1 2017 2017
CUI: C4285782
Disease: Kinesiophobia
Kinesiophobia 		disease Disease or Syndrome 14 1 0.010 None 1.000 1 2019 2019
CUI: C0751885
Disease: Myasthenic Syndromes, Congenital, Slow Channel
Myasthenic Syndromes, Congenital, Slow Channel 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 18 1 0.010 None < 0.001 1 2002 2002
CUI: C1709661
Disease: Primary Focal Segmental Glomerulosclerosis
Primary Focal Segmental Glomerulosclerosis 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 18 0.010 None 1.000 1 2003 2003
CUI: C1737225
Disease: Mesangioproliferative glomerulonephritis
Mesangioproliferative glomerulonephritis 		disease Disease or Syndrome 21 0.010 None 1.000 1 2004 2004
CUI: C1305904
Disease: Familial hematuria
Familial hematuria 		disease Disease or Syndrome 23 7 0.010 None 1.000 1 2018 2018
CUI: C2242817
Disease: Homocysteine measurement
Homocysteine measurement 		phenotype Laboratory Procedure 23 33 0.100 None 1.000 1 1 2016 2016
CUI: C0086432
Disease: Hyalinosis, Segmental Glomerular
Hyalinosis, Segmental Glomerular 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 28 0.300 None 0
CUI: C3714731
Disease: Early childhood caries
Early childhood caries 		disease Stomatognathic Diseases Disease or Syndrome 30 8 0.010 None 1.000 1 2017 2017
CUI: C1868672
Disease: NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE
NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 31 53 0.300 None 1.000 1 2007 2007
CUI: C3501848
Disease: Nephrosis, congenital
Nephrosis, congenital 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 31 9 0.010 None 1.000 1 2003 2003
CUI: C0022972
Disease: Lambert-Eaton Myasthenic Syndrome
Lambert-Eaton Myasthenic Syndrome 		disease Neoplasms; Immune System Diseases; Nervous System Diseases Disease or Syndrome 37 1 0.010 None 1.000 1 2018 2018
CUI: C0009088
Disease: Cluster Headache
Cluster Headache 		disease Nervous System Diseases Disease or Syndrome 38 13 0.010 None 1.000 1 2017 2017
CUI: C0027341
Disease: Nail-Patella Syndrome
Nail-Patella Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 38 18 0.010 None < 0.001 1 2003 2003
CUI: C0016052
Disease: Fibromuscular Dysplasia
Fibromuscular Dysplasia 		disease Cardiovascular Diseases Disease or Syndrome 47 3 0.010 None 1.000 1 2020 2020
CUI: C0751882
Disease: Myasthenic Syndromes, Congenital
Myasthenic Syndromes, Congenital 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 57 40 0.050 None 1.000 5 2003 2019
CUI: C0403397
Disease: Steroid-resistant nephrotic syndrome
Steroid-resistant nephrotic syndrome 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 73 25 0.020 None 1.000 2 2010 2014