CRYGD, crystallin gamma D, 1421

N. diseases: 168; N. variants: 18
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: C3540850
Disease: CATARACT 4, MULTIPLE TYPES
CATARACT 4, MULTIPLE TYPES 		disease Disease or Syndrome 1 6 0.900 None 1.000 12 6 1999 2011
CUI: C0086543
Disease: Cataract
Cataract 		disease Eye Diseases Acquired Abnormality 878 124 0.700 strong 0.960 25 8 1999 2019
CUI: C1852438
Disease: CATARACT, COPPOCK-LIKE
CATARACT, COPPOCK-LIKE 		disease Eye Diseases Disease or Syndrome 20 1 0.500 None 1.000 2 2000 2011
CUI: C0009691
Disease: Congenital cataract
Congenital cataract 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Eye Diseases; Nervous System Diseases Congenital Abnormality 105 104 0.400 None 1.000 19 7 2000 2019
CUI: C1392104
Disease: Coralliform cataract
Coralliform cataract 		disease Eye Diseases Congenital Abnormality 2 3 0.330 None 1.000 4 3 2004 2013
CUI: C0392557
Disease: Nuclear cataract
Nuclear cataract 		disease Eye Diseases Disease or Syndrome 39 11 0.320 None 1.000 4 2006 2015
CUI: C1112705
Disease: Nuclear non-senile cataract
Nuclear non-senile cataract 		disease Eye Diseases Disease or Syndrome 69 11 0.320 None 1.000 4 2006 2015
CUI: C1858679
Disease: CATARACT, AUTOSOMAL DOMINANT
CATARACT, AUTOSOMAL DOMINANT 		disease Eye Diseases Disease or Syndrome 14 10 0.310 strong 1.000 2 1999 2010
CUI: C1861832
Disease: CATARACT, CRYSTALLINE ACULEIFORM
CATARACT, CRYSTALLINE ACULEIFORM 		phenotype Eye Diseases Finding 1 4 0.300 None 1.000 10 4 1999 2017
CUI: C0524524
Disease: Pseudoaphakia
Pseudoaphakia 		disease Eye Diseases Disease or Syndrome 28 0.300 None 1.000 2 1999 2018
CUI: C1510497
Disease: Lens Opacities
Lens Opacities 		phenotype Eye Diseases Finding 24 0.300 None 1.000 2 1999 2018
CUI: C0344523
Disease: Cataract, congenital, cerulean type 1
Cataract, congenital, cerulean type 1 		disease Eye Diseases Congenital Abnormality 6 0.300 None 1.000 1 2003 2003
CUI: C1833118
Disease: Cataract, Pulverulent
Cataract, Pulverulent 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 12 4 0.300 None 1.000 1 2011 2011
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly 		phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Finding 523 30 0.300 None 1.000 1 2017 2017
CUI: C1861829
Disease: Cataract microcornea syndrome
Cataract microcornea syndrome 		disease Eye Diseases Disease or Syndrome 10 5 0.300 None 1.000 1 2007 2007
CUI: C3888391
Disease: Nonnuclear polymorphic congenital cataract
Nonnuclear polymorphic congenital cataract 		disease Congenital Abnormality 71 0.210 None 1.000 2 2002 2018
CUI: C3888390
Disease: Cataract, Punctate, Progressive Juvenile-Onset
Cataract, Punctate, Progressive Juvenile-Onset 		disease Eye Diseases Disease or Syndrome 1 0.200 None 1.000 1 2002 2002
CUI: C0029531
Disease: Other cataract
Other cataract 		disease Eye Diseases Disease or Syndrome 32 0.200 None 1.000 1 1994 1994
CUI: C1837023
Disease: CATARACT, CONGENITAL, CERULEAN TYPE, 3
CATARACT, CONGENITAL, CERULEAN TYPE, 3 		disease Eye Diseases Disease or Syndrome 1 0.200 None 1.000 1 2002 2002
CUI: C4721890
Disease: CATARACT 2, MULTIPLE TYPES
CATARACT 2, MULTIPLE TYPES 		disease Disease or Syndrome 3 6 0.200 None 1.000 1 2000 2000
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases Disease or Syndrome 2723 2387 0.100 None 0.927 123 2005 2020
CUI: C4551683
Disease: Adrenal Gland Pheochromocytoma
Adrenal Gland Pheochromocytoma 		disease Neoplasms; Endocrine System Diseases Neoplastic Process 416 50 0.100 None 0.909 11 2010 2019
CUI: C0027651
Disease: Neoplasms
Neoplasms 		group Neoplasms Neoplastic Process 10161 1644 0.100 None 1.000 10 2010 2019
CUI: C0027092
Disease: Myopia
Myopia 		disease Eye Diseases Disease or Syndrome 490 167 0.100 None 0
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity 		phenotype Eye Diseases Finding 113 5 0.100 None 0