NRP1, neuropilin 1, 8829

N. diseases: 246; N. variants: 13
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: C1832274
Disease: Charcot-Marie-Tooth disease, Type 2D
Charcot-Marie-Tooth disease, Type 2D 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 5 9 0.010 None 1.000 1 2018 2018
CUI: C0339296
Disease: Neurotrophic keratitis
Neurotrophic keratitis 		disease Eye Diseases; Nervous System Diseases; Stomatognathic Diseases Disease or Syndrome 7 0.010 None 1.000 1 2019 2019
CUI: C0027858
Disease: Neuroma
Neuroma 		disease Neoplasms Neoplastic Process 15 0.010 None 1.000 1 2007 2007
CUI: C0027686
Disease: Pathologic Neovascularization
Pathologic Neovascularization 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 16 0.010 None 1.000 1 2006 2006
CUI: C0334608
Disease: Angiomatous Meningioma
Angiomatous Meningioma 		disease Neoplasms; Nervous System Diseases Neoplastic Process 18 0.020 None 1.000 2 2013 2013
CUI: C4068858
Disease: Avascular retina
Avascular retina 		disease Disease or Syndrome 19 0.010 None 1.000 1 2010 2010
CUI: C3826457
Disease: Diabetes in children
Diabetes in children 		disease Disease or Syndrome 22 2 0.010 None 1.000 1 2010 2010
CUI: C0085625
Disease: Hypoalgesia
Hypoalgesia 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders Sign or Symptom 23 7 0.010 None 1.000 1 2011 2011
CUI: C3267003
Disease: Vascular endothelial growth factor overexpression
Vascular endothelial growth factor overexpression 		disease Disease or Syndrome 26 0.010 None 1.000 1 2000 2000
CUI: C3276706
Disease: Small Fiber Neuropathy
Small Fiber Neuropathy 		disease Nervous System Diseases Disease or Syndrome 35 8 0.010 None 1.000 1 2016 2016
CUI: C0025048
Disease: Meconium Aspiration Syndrome
Meconium Aspiration Syndrome 		phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Respiratory Tract Diseases Disease or Syndrome 38 1 0.020 None 0.500 2 2018 2018
CUI: C0042344
Disease: Varicose Ulcer
Varicose Ulcer 		disease Skin and Connective Tissue Diseases; Cardiovascular Diseases Disease or Syndrome 38 2 0.010 None 1.000 1 2008 2008
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		disease Disease or Syndrome 39 5 0.010 None 1.000 1 2020 2020
CUI: C0023223
Disease: Leg Ulcer
Leg Ulcer 		disease Skin and Connective Tissue Diseases Disease or Syndrome 40 0.010 None 1.000 1 2008 2008
CUI: C0015826
Disease: Fenestration (morphologic abnormality)
Fenestration (morphologic abnormality) 		disease Acquired Abnormality 43 0.010 None 1.000 1 2019 2019
CUI: C0699753
Disease: Cancer Relapse
Cancer Relapse 		disease Neoplastic Process 48 0.020 None 1.000 2 2007 2019
CUI: C0024620
Disease: Primary Malignant Liver Neoplasm
Primary Malignant Liver Neoplasm 		disease Digestive System Diseases; Neoplasms Neoplastic Process 60 4 0.010 None 1.000 1 2018 2018
CUI: C0014599
Disease: Epithelial hyperplasia
Epithelial hyperplasia 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 63 0.010 None 1.000 1 2002 2002
CUI: C0346976
Disease: Secondary malignant neoplasm of pancreas
Secondary malignant neoplasm of pancreas 		disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 69 4 0.010 None 1.000 1 2019 2019
CUI: C3495949
Disease: Locally advanced breast cancer
Locally advanced breast cancer 		disease Neoplastic Process 71 3 0.010 None 1.000 1 2019 2019
CUI: C1840311
Disease: Laryngeal cleft
Laryngeal cleft 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 72 4 0.010 None 1.000 1 2018 2018
CUI: C0086565
Disease: Liver Dysfunction
Liver Dysfunction 		phenotype Digestive System Diseases Finding 73 0.300 None 1.000 1 2010 2010
CUI: C0041207
Disease: Truncus Arteriosus, Persistent
Truncus Arteriosus, Persistent 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 76 4 0.010 None 1.000 1 2015 2015
CUI: C0035328
Disease: Retinal Vein Occlusion
Retinal Vein Occlusion 		disease Eye Diseases; Cardiovascular Diseases Disease or Syndrome 76 15 0.200 None 0
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 86 30 0.010 None 1.000 1 2011 2011