FGF13, fibroblast growth factor 13, 2258

N. diseases: 167; N. variants: 1
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: C1519172
Disease: Salivary Gland Carcinoma ex Pleomorphic Adenoma
Salivary Gland Carcinoma ex Pleomorphic Adenoma 		disease Neoplastic Process 4 0.010 None 1.000 1 2010 2010
CUI: C4324434
Disease: Panniculus
Panniculus 		disease Disease or Syndrome 4 0.010 None 1.000 1 2020 2020
CUI: C4087491
Disease: End stage COPD
End stage COPD 		disease Disease or Syndrome 5 0.010 None 1.000 1 2017 2017
CUI: C0332877
Disease: Congenital premature fusion
Congenital premature fusion 		disease Congenital Abnormality 6 1 0.010 None 1.000 1 2005 2005
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 8 36 0.010 None 1.000 1 2001 2001
CUI: C1335965
Disease: Signet-ring cell adenocarcinoma gastric
Signet-ring cell adenocarcinoma gastric 		disease Neoplasms Neoplastic Process 8 0.010 None 1.000 1 2018 2018
CUI: C0265339
Disease: Borjeson-Forssman-Lehmann syndrome
Borjeson-Forssman-Lehmann syndrome 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 9 15 0.010 None 1.000 1 1999 1999
CUI: C1300257
Disease: Thanatophoric dysplasia, type 2
Thanatophoric dysplasia, type 2 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 11 17 0.010 None 1.000 1 2014 2014
CUI: C0034535
Disease: Radiation Syndrome
Radiation Syndrome 		disease Wounds and Injuries Disease or Syndrome 14 0.010 None 1.000 1 2019 2019
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 20 24 0.010 None 1.000 1 2001 2001
CUI: C4025218
Disease: Vasculitis of large artery
Vasculitis of large artery 		disease Cardiovascular Diseases Disease or Syndrome 21 0.010 None 1.000 1 2019 2019
CUI: C1855900
Disease: HYPERTRICHOSIS, CONGENITAL GENERALIZED
HYPERTRICHOSIS, CONGENITAL GENERALIZED 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 25 0.010 None 1.000 1 2013 2013
CUI: C0344460
Disease: Carcinoma ex pleomorphic adenoma
Carcinoma ex pleomorphic adenoma 		disease Neoplasms; Stomatognathic Diseases Neoplastic Process 30 2 0.010 None 1.000 1 2010 2010
CUI: C0333293
Disease: Healing ulcer
Healing ulcer 		disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 43 1 0.010 None 1.000 1 2005 2005
CUI: C1860707
Disease: TUBEROUS SCLEROSIS 2 (disorder)
TUBEROUS SCLEROSIS 2 (disorder) 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases Disease or Syndrome 43 255 0.010 None 1.000 1 2010 2010
CUI: C0032969
Disease: Pregnancy in Diabetics
Pregnancy in Diabetics 		phenotype Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 53 1 0.010 None 1.000 1 1998 1998
CUI: C0021775
Disease: Intermittent Claudication
Intermittent Claudication 		phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 60 69 0.010 None 1.000 1 2009 2009
CUI: C1519176
Disease: Salivary Gland Pleomorphic Adenoma
Salivary Gland Pleomorphic Adenoma 		disease Neoplasms; Stomatognathic Diseases Neoplastic Process 63 9 0.010 None 1.000 1 2012 2012
CUI: C1859592
Disease: ATRICHIA WITH PAPULAR LESIONS
ATRICHIA WITH PAPULAR LESIONS 		disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 70 3 0.010 None 1.000 1 2005 2005
CUI: C0410480
Disease: Avascular Necrosis of Femur Head
Avascular Necrosis of Femur Head 		phenotype Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Disease or Syndrome 74 20 0.020 None 1.000 2 2018 2019
CUI: C0151846
Disease: Periosteal Disorder
Periosteal Disorder 		disease Musculoskeletal Diseases Disease or Syndrome 80 0.010 None 1.000 1 2018 2018
CUI: C1519666
Disease: Tumor-Associated Vasculature
Tumor-Associated Vasculature 		disease Acquired Abnormality 84 0.010 None 1.000 1 2008 2008
CUI: C0595936
Disease: Aqueous Humor Disorders
Aqueous Humor Disorders 		disease Eye Diseases Disease or Syndrome 85 1 0.010 None 1.000 1 2017 2017
CUI: C1510885
Disease: Angiogenic Switch
Angiogenic Switch 		disease Neoplastic Process 96 3 0.010 None 1.000 1 2009 2009
CUI: C1168327
Disease: High-Grade Prostatic Intraepithelial Neoplasia
High-Grade Prostatic Intraepithelial Neoplasia 		disease Neoplasms; Male Urogenital Diseases Neoplastic Process 111 0.010 None 1.000 1 2016 2016