CDKN2D, cyclin dependent kinase inhibitor 2D, 1032

N. diseases: 110; N. variants: 2
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: C0275911
Disease: Tuberculosis of intestines
Tuberculosis of intestines 		disease Digestive System Diseases; Infections Disease or Syndrome 24 2 0.010 None 1.000 1 2013 2013
CUI: C0375019
Disease: Human T-cell lymphotrophic virus, type I [HTLV-I]
Human T-cell lymphotrophic virus, type I [HTLV-I] 		disease Disease or Syndrome 25 0.010 None 1.000 1 2012 2012
CUI: C0280216
Disease: stage, neuroblastoma
stage, neuroblastoma 		disease Neoplasms Neoplastic Process 27 4 0.010 None 1.000 1 2004 2004
CUI: C1332969
Disease: Childhood Ganglioglioma
Childhood Ganglioglioma 		disease Neoplasms Neoplastic Process 38 4 0.010 None 1.000 1 2007 2007
CUI: C0339508
Disease: Hereditary macular dystrophy
Hereditary macular dystrophy 		disease Congenital Abnormality 39 10 0.010 None 1.000 1 2018 2018
CUI: C0017150
Disease: Gastrinoma
Gastrinoma 		disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 49 0.010 None 1.000 1 2001 2001
CUI: C0587248
Disease: Costello syndrome (disorder)
Costello syndrome (disorder) 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 50 24 0.010 None 1.000 1 2015 2015
CUI: C0014743
Disease: Erythema Nodosum
Erythema Nodosum 		disease Skin and Connective Tissue Diseases; Immune System Diseases; Chemically-Induced Disorders Disease or Syndrome 51 3 0.010 None 1.000 1 2008 2008
CUI: C0730292
Disease: Macular dystrophy
Macular dystrophy 		disease Eye Diseases Disease or Syndrome 52 59 0.010 None 1.000 1 2018 2018
CUI: C0339789
Disease: Congenital deafness
Congenital deafness 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Nervous System Diseases; Otorhinolaryngologic Diseases Congenital Abnormality 72 11 0.010 None 1.000 1 2011 2011
CUI: C0406317
Disease: Chronic small plaque psoriasis
Chronic small plaque psoriasis 		disease Skin and Connective Tissue Diseases Disease or Syndrome 82 3 0.040 None 1.000 4 2017 2019
CUI: C0005956
Disease: Bone Marrow Diseases
Bone Marrow Diseases 		group Hemic and Lymphatic Diseases Disease or Syndrome 84 3 0.010 None 1.000 1 1992 1992
CUI: C0037928
Disease: Spinal Cord Diseases
Spinal Cord Diseases 		group Nervous System Diseases Disease or Syndrome 84 3 0.010 None 1.000 1 1992 1992
CUI: C0030481
Disease: Tropical Spastic Paraparesis
Tropical Spastic Paraparesis 		disease Infections; Nervous System Diseases Disease or Syndrome 88 4 0.010 None 1.000 1 1992 1992
CUI: C0206716
Disease: Ganglioglioma
Ganglioglioma 		disease Neoplasms Neoplastic Process 91 7 0.010 None 1.000 1 2007 2007
CUI: C4725671
Disease: High-Risk Neuroblastoma
High-Risk Neuroblastoma 		disease Neoplasms Neoplastic Process 99 4 0.010 None 1.000 1 2017 2017
CUI: C0262587
Disease: Parathyroid Adenoma
Parathyroid Adenoma 		disease Neoplasms; Endocrine System Diseases Neoplastic Process 133 12 0.010 None 1.000 1 2013 2013
CUI: C0206664
Disease: Teratocarcinoma
Teratocarcinoma 		disease Neoplasms Neoplastic Process 141 1 0.050 None 1.000 5 2003 2019
CUI: C0206659
Disease: Embryonal Carcinoma
Embryonal Carcinoma 		disease Neoplasms Neoplastic Process 165 0.100 None 1.000 14 1992 2019
CUI: C0349639
Disease: Juvenile Myelomonocytic Leukemia
Juvenile Myelomonocytic Leukemia 		disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 179 70 0.010 None 1.000 1 2011 2011
CUI: C0033036
Disease: Atrial Premature Complexes
Atrial Premature Complexes 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 183 21 0.010 None 1.000 1 2013 2013
CUI: C0238790
Disease: bone destruction
bone destruction 		disease Disease or Syndrome 234 3 0.010 None 1.000 1 1989 1989
CUI: C0002874
Disease: Aplastic Anemia
Aplastic Anemia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 238 30 0.010 None 1.000 1 2009 2009
CUI: C2745900
Disease: Promyelocytic leukemia
Promyelocytic leukemia 		disease Neoplastic Process 255 2 0.030 None 1.000 3 1988 2019
CUI: C0263361
Disease: Psoriasis vulgaris
Psoriasis vulgaris 		disease Skin and Connective Tissue Diseases Disease or Syndrome 255 80 0.010 None 1.000 1 2004 2004