LAD1, ladinin 1, 3898

N. diseases: 87; 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: C0432326
Disease: Junctional epidermolysis bullosa mitis
Junctional epidermolysis bullosa mitis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Congenital Abnormality 2 0.010 None 1.000 1 1997 1997
CUI: C0935560
Disease: Multiple disability
Multiple disability 		disease Disease or Syndrome 2 1 0.010 None 1.000 1 2020 2020
CUI: C0340319
Disease: Posterior myocardial infarction
Posterior myocardial infarction 		phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 3 0.010 None < 0.001 1 2017 2017
CUI: C0406650
Disease: Linear IgA Bullous Dermatosis
Linear IgA Bullous Dermatosis 		disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 4 0.030 None 1.000 3 1997 2017
CUI: C0264695
Disease: Subendocardial ischemia
Subendocardial ischemia 		phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 4 0.010 None 1.000 1 2019 2019
CUI: C0856737
Disease: Single vessel disease
Single vessel disease 		disease Cardiovascular Diseases Disease or Syndrome 6 0.010 None 1.000 1 2018 2018
CUI: C2748536
Disease: Leukocyte Adhesion Deficiency, Type III
Leukocyte Adhesion Deficiency, Type III 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases Disease or Syndrome 7 6 0.010 None 1.000 1 2010 2010
CUI: C0398739
Disease: Congenital disorder of glycosylation, type 2C
Congenital disorder of glycosylation, type 2C 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 9 6 0.050 None 1.000 5 1998 2001
CUI: C0399451
Disease: Subgingival plaque
Subgingival plaque 		disease Stomatognathic Diseases Disease or Syndrome 9 0.010 None 1.000 1 2015 2015
CUI: C1852540
Disease: Coronary Artery Dissection, Spontaneous
Coronary Artery Dissection, Spontaneous 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 11 0.010 None 1.000 1 2019 2019
CUI: C0265191
Disease: Chronic acquired lymphedema
Chronic acquired lymphedema 		disease Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases Disease or Syndrome 12 0.010 None 1.000 1 2017 2017
CUI: C1264606
Disease: Persistent infection
Persistent infection 		phenotype Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 13 0.020 None 1.000 2 1999 2001
CUI: C0272187
Disease: Congenital leukocyte adherence deficiency
Congenital leukocyte adherence deficiency 		disease Disease or Syndrome 14 12 0.100 None 1.000 15 1998 2015
CUI: C0079301
Disease: Junctional Epidermolysis Bullosa
Junctional Epidermolysis Bullosa 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 16 9 0.020 None 1.000 2 1997 1998
CUI: C0030804
Disease: Pemphigoid, Benign Mucous Membrane
Pemphigoid, Benign Mucous Membrane 		disease Eye Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 19 1 0.010 None 1.000 1 2006 2006
CUI: C0342783
Disease: Deficiency of butyryl-CoA dehydrogenase
Deficiency of butyryl-CoA dehydrogenase 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 21 47 0.010 None 1.000 1 2017 2017
CUI: C0036221
Disease: Mast-Cell Sarcoma
Mast-Cell Sarcoma 		disease Neoplasms Neoplastic Process 27 4 0.010 None 1.000 1 2003 2003
CUI: C0398368
Disease: Lymphatic Abnormalities
Lymphatic Abnormalities 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Anatomical Abnormality 30 6 0.010 None 1.000 1 2017 2017
CUI: C3275069
Disease: Chronic Total Occlusion Vessel
Chronic Total Occlusion Vessel 		disease Disease or Syndrome 33 0.010 None < 0.001 1 2006 2006
CUI: C0206064
Disease: Microvascular Angina
Microvascular Angina 		disease Cardiovascular Diseases Disease or Syndrome 39 10 0.010 None 1.000 1 2017 2017
CUI: C1739108
Disease: Latent Autoimmune Diabetes in Adults
Latent Autoimmune Diabetes in Adults 		disease Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome 39 12 0.010 None 1.000 1 2017 2017
CUI: C0014527
Disease: Epidermolysis Bullosa
Epidermolysis Bullosa 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Congenital Abnormality 47 3 0.010 None 1.000 1 1998 1998
CUI: C0085652
Disease: Pyoderma Gangrenosum
Pyoderma Gangrenosum 		disease Skin and Connective Tissue Diseases Disease or Syndrome 47 2 0.010 None 1.000 1 2015 2015
CUI: C0040015
Disease: Thrombasthenia
Thrombasthenia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 48 61 0.010 None 1.000 1 2009 2009
CUI: C0020452
Disease: Hyperemia
Hyperemia 		disease Cardiovascular Diseases Disease or Syndrome 64 3 0.010 None 1.000 1 2019 2019