FLT1, fms related receptor tyrosine kinase 1, 2321

N. diseases: 424; N. variants: 33
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: C0266752
Disease: Twin placenta
Twin placenta 		disease Anatomical Abnormality 2 0.010 None 1.000 1 2013 2013
CUI: C0877550
Disease: Carcinomatous ascites
Carcinomatous ascites 		disease Neoplastic Process 2 0.010 None 1.000 1 2002 2002
CUI: C0015366
Disease: Extramedullary hematopoiesis of spleen
Extramedullary hematopoiesis of spleen 		disease Hemic and Lymphatic Diseases Disease or Syndrome 3 0.010 None 1.000 1 2019 2019
CUI: C4024994
Disease: Abnormality of the hepatic vasculature
Abnormality of the hepatic vasculature 		phenotype Anatomical Abnormality 3 0.100 None 0
CUI: C0346975
Disease: Secondary malignant neoplasm of rectum
Secondary malignant neoplasm of rectum 		disease Digestive System Diseases; Neoplasms Neoplastic Process 4 0.010 None 1.000 1 2018 2018
CUI: C0861772
Disease: Stage IV Rectal Carcinoma
Stage IV Rectal Carcinoma 		disease Neoplastic Process 4 0.010 None 1.000 1 2018 2018
CUI: C2609079
Disease: Mirror syndrome
Mirror syndrome 		disease Disease or Syndrome 4 0.010 None 1.000 1 2020 2020
CUI: C0231254
Disease: Increased body mass index
Increased body mass index 		phenotype Finding 4 0.100 None 0
CUI: C0334511
Disease: Pleural Solitary Fibrous Tumor
Pleural Solitary Fibrous Tumor 		disease Neoplasms Neoplastic Process 5 3 0.010 None 1.000 1 2 2018 2018
CUI: C1306893
Disease: Anomaly of placenta
Anomaly of placenta 		phenotype Female Urogenital Diseases and Pregnancy Complications Pathologic Function 5 0.100 None 0
CUI: C1336257
Disease: Stage 3 Neuroblastoma
Stage 3 Neuroblastoma 		disease Neoplasms Neoplastic Process 6 0.010 None 1.000 1 2002 2002
CUI: C1838163
Disease: OSLER-RENDU-WEBER SYNDROME 2
OSLER-RENDU-WEBER SYNDROME 2 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Cardiovascular Diseases Disease or Syndrome 6 91 0.010 None 1.000 1 2018 2018
CUI: C4692625
Disease: SHWACHMAN-DIAMOND SYNDROME 1
SHWACHMAN-DIAMOND SYNDROME 1 		disease Disease or Syndrome 7 14 0.010 None 1.000 1 2004 2004
CUI: C0002351
Disease: Altitude Sickness
Altitude Sickness 		phenotype Respiratory Tract Diseases Disease or Syndrome 10 0.010 None 1.000 1 2005 2005
CUI: C1281300
Disease: Vascular degeneration
Vascular degeneration 		disease Cardiovascular Diseases Disease or Syndrome 10 1 0.010 None 1.000 1 2003 2003
CUI: C0272394
Disease: Disorder of lymph node
Disorder of lymph node 		group Hemic and Lymphatic Diseases Disease or Syndrome 11 0.010 None 1.000 1 2017 2017
CUI: C0796466
Disease: Refractory cytopenia with multilineage dysplasia
Refractory cytopenia with multilineage dysplasia 		disease Hemic and Lymphatic Diseases Neoplastic Process 11 1 0.010 None 1.000 1 2013 2013
CUI: C3840252
Disease: Pseudomyogenic (epithelioid sarcoma-like) hemangioendothelioma
Pseudomyogenic (epithelioid sarcoma-like) hemangioendothelioma 		disease Neoplastic Process 12 0.010 None 1.000 1 2018 2018
CUI: C1306571
Disease: Hepatic Insufficiency
Hepatic Insufficiency 		phenotype Digestive System Diseases Pathologic Function 13 0.010 None 1.000 1 2008 2008
CUI: C4684861
Disease: Recurrent Malignant Glioma
Recurrent Malignant Glioma 		disease Neoplasms Neoplastic Process 13 0.010 None 1.000 1 2017 2017
CUI: C1840374
Disease: Elevated systolic blood pressure
Elevated systolic blood pressure 		phenotype Cardiovascular Diseases Finding 14 1 0.100 None 0
CUI: C1840375
Disease: Elevated diastolic blood pressure
Elevated diastolic blood pressure 		phenotype Cardiovascular Diseases Finding 14 1 0.100 None 0
CUI: C0220624
Disease: Adult Brain Neoplasm
Adult Brain Neoplasm 		disease Neoplasms; Nervous System Diseases Neoplastic Process 15 0.010 None 1.000 1 2017 2017
CUI: C4551479
Disease: Schwartz-Jampel Syndrome, Type 1
Schwartz-Jampel Syndrome, Type 1 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 16 4 0.300 None 1.000 1 2007 2007
CUI: C1853578
Disease: Neuroferritinopathy
Neuroferritinopathy 		disease Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 17 5 0.010 None 1.000 1 2015 2015