FLVCR1, FLVCR heme transporter 1, 28982

N. diseases: 188; N. variants: 12
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: C1836916
Disease: POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA
POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases Disease or Syndrome 1 6 0.760 None 1.000 7 6 2010 2018
CUI: C0233737
Disease: Circumlocution
Circumlocution 		disease Mental or Behavioral Dysfunction 1 0.010 None 1.000 1 2018 2018
CUI: C4022421
Disease: Abnormal sensory nerve conduction velocity
Abnormal sensory nerve conduction velocity 		phenotype Finding 1 0.100 None 0
CUI: C1867923
Disease: Posterior column ataxia
Posterior column ataxia 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 2 0.060 None 1.000 6 2010 2019
CUI: C0265097
Disease: Basilar Artery Stenosis
Basilar Artery Stenosis 		disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C0426908
Disease: Telescoping of limb at hip
Telescoping of limb at hip 		phenotype Sign or Symptom 2 0.010 None 1.000 1 2018 2018
CUI: C0867390
Disease: postoperative stroke
postoperative stroke 		disease Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C1263853
Disease: Paralytic stroke
Paralytic stroke 		disease Nervous System Diseases; Mental Disorders; Cardiovascular Diseases Disease or Syndrome 2 0.010 None 1.000 1 2020 2020
CUI: C3203738
Disease: Fowler syndrome
Fowler syndrome 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 2 1 0.010 None 1.000 1 2010 2010
CUI: C0438434
Disease: Scotoma, Ring
Scotoma, Ring 		phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Sign or Symptom 2 0.100 None 0
CUI: C0085164
Disease: Leukemia, Feline
Leukemia, Feline 		disease Neoplasms; Infections; Animal Diseases Neoplastic Process 3 0.010 None 1.000 1 2006 2006
CUI: C0265098
Disease: Basilar artery occlusion
Basilar artery occlusion 		disease Nervous System Diseases; Cardiovascular Diseases Anatomical Abnormality 4 0.010 None 1.000 1 2018 2018
CUI: C4274665
Disease: Logopenic progressive aphasia
Logopenic progressive aphasia 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Mental or Behavioral Dysfunction 4 0.010 None 1.000 1 2017 2017
CUI: C4025722
Disease: Abnormality of the spinal cord
Abnormality of the spinal cord 		group Finding 4 0.100 None 0
CUI: C2674512
Disease: Truncal titubation
Truncal titubation 		phenotype Finding 5 2 0.100 None 0
CUI: C0520904
Disease: Postoperative Nausea
Postoperative Nausea 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 7 1 0.010 None 1.000 1 2019 2019
CUI: C2215257
Disease: Acute postoperative pain
Acute postoperative pain 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 8 0.010 None 1.000 1 2018 2018
CUI: C0016204
Disease: Flatulence
Flatulence 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 11 0.010 None 1.000 1 2017 2017
CUI: C0240914
Disease: Romberg's sign positive
Romberg's sign positive 		phenotype Finding 15 6 0.100 None 0
CUI: C1849148
Disease: Decreased sensory nerve conduction velocity
Decreased sensory nerve conduction velocity 		phenotype Finding 15 0.100 None 0
CUI: C0002892
Disease: Anemia, Pernicious
Anemia, Pernicious 		disease Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 16 4 0.010 None 1.000 1 2015 2015
CUI: C1837496
Disease: Axonal degeneration
Axonal degeneration 		phenotype Finding 17 0.100 None 0
CUI: C1857304
Disease: Flexion contracture of finger
Flexion contracture of finger 		phenotype Finding 17 4 0.100 None 0
CUI: C0036454
Disease: Scotoma
Scotoma 		phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Finding 21 0.100 None 0
CUI: C0036996
Disease: Short Rib-Polydactyly Syndrome
Short Rib-Polydactyly Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 21 13 0.100 None 0 1