AHSG, alpha 2-HS glycoprotein, 197

N. diseases: 204; 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.
Alopecia-Mental Retardation Syndrome 1
disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Disease or Syndrome 1 1 0.500 None 1.000 1 1 2017 2017
CUI: C4268640
Disease: Mixed irritable bowel syndrome
Mixed irritable bowel syndrome
disease Digestive System Diseases Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C0014571
Disease: Epiphyses, Slipped
Epiphyses, Slipped
disease Musculoskeletal Diseases Disease or Syndrome 2 1 0.010 None 1.000 1 2017 2017
Perniola Krajewska Carnevale syndrome
disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Disease or Syndrome 2 0.300 None 1.000 1 2017 2017
CUI: C4551986
Disease: AMR Syndrome
AMR Syndrome
disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Disease or Syndrome 2 0.310 None 1.000 1 2017 2017
CUI: C4021902
Disease: Short corpus callosum
Short corpus callosum
disease Anatomical Abnormality 3 0.100 None 0
CUI: C0020497
Disease: Cortical Congenital Hyperostosis
Cortical Congenital Hyperostosis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 5 10 0.010 None 1.000 1 2019 2019
CUI: C0036091
Disease: Sialolithiasis
Sialolithiasis
disease Pathological Conditions, Signs and Symptoms; Stomatognathic Diseases Disease or Syndrome 5 0.010 None 1.000 1 2017 2017
CUI: C0729665
Disease: Arteriovenous graft
Arteriovenous graft
disease Acquired Abnormality 10 2 0.010 None 1.000 1 2018 2018
CUI: C0005866
Disease: Bluetongue infection
Bluetongue infection
disease Infections; Animal Diseases Disease or Syndrome 13 0.010 None 1.000 1 2018 2018
CUI: C0861155
Disease: Rhinoconjunctivitis
Rhinoconjunctivitis
disease Eye Diseases Disease or Syndrome 14 16 0.010 None 1.000 1 2017 2017
CUI: C0740919
Disease: Allergy to grass pollen
Allergy to grass pollen
disease Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 17 0.010 None 1.000 1 2017 2017
CUI: C4042861
Disease: Obesity, Metabolically Benign
Obesity, Metabolically Benign
phenotype Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Sign or Symptom 19 8 0.010 None 1.000 1 2018 2018
CUI: C0263505
Disease: Alopecia universalis
Alopecia universalis
disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 19 2 0.100 None 0
CUI: C0205710
Disease: Alpers Syndrome (disorder)
Alpers Syndrome (disorder)
disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 28 128 0.020 None 1.000 2 2013 2016
CUI: C1960636
Disease: Dysglycemia
Dysglycemia
disease Disease or Syndrome 31 2 0.010 None 1.000 1 2018 2018
CUI: C0037036
Disease: Sialorrhea
Sialorrhea
disease Stomatognathic Diseases Disease or Syndrome 32 1 0.010 None < 0.001 1 2016 2016
CUI: C1833683
Disease: NEPHROLITHIASIS, CALCIUM OXALATE
NEPHROLITHIASIS, CALCIUM OXALATE
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 33 30 0.110 None 1.000 2 2 2010 2014
CUI: C4025252
Disease: Abnormal nasal morphology
Abnormal nasal morphology
disease Anatomical Abnormality 34 0.100 None 0
CUI: C0432306
Disease: Ichthyosis Bullosa of Siemens
Ichthyosis Bullosa of Siemens
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Congenital Abnormality 37 12 0.010 None 1.000 1 2017 2017
CUI: C0473583
Disease: Nevus elasticus
Nevus elasticus
disease Neoplasms Neoplastic Process 37 5 0.010 None 1.000 1 2006 2006
CUI: C0521174
Disease: Microcalcification
Microcalcification
phenotype Nutritional and Metabolic Diseases Pathologic Function 42 0.300 None 1.000 1 2005 2005
CUI: C0263628
Disease: Tumoral calcinosis
Tumoral calcinosis
disease Nutritional and Metabolic Diseases Disease or Syndrome 45 3 0.300 None 1.000 1 2005 2005
Intellectual disability, progressive
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Finding 45 1 0.100 None 0
CUI: C0431129
Disease: Adamantinous Craniopharyngioma
Adamantinous Craniopharyngioma
disease Neoplasms Neoplastic Process 48 6 0.010 None 1.000 1 2017 2017