FOXE1, forkhead box E1, 2304

N. diseases: 102; 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: C1855794
Disease: Bamforth syndrome
Bamforth syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Endocrine System Diseases; Stomatognathic Diseases Disease or Syndrome 6 3 0.930 None 1.000 8 3 1998 2014
CUI: C0010308
Disease: Congenital Hypothyroidism
Congenital Hypothyroidism
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases Disease or Syndrome 94 48 0.700 strong 1.000 14 1 2002 2017
CUI: C4225293
Disease: THYROID CANCER, NONMEDULLARY, 4
THYROID CANCER, NONMEDULLARY, 4
disease Neoplastic Process 1 1 0.700 moderate 1.000 1 1 2015 2015
CUI: C0749420
Disease: Thyroid Agenesis
Thyroid Agenesis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases Congenital Abnormality 11 3 0.650 strong 1.000 5 2 1998 2017
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
disease Neoplasms; Endocrine System Diseases Neoplastic Process 1348 204 0.500 None 1.000 24 3 2001 2019
CUI: C0008925
Disease: Cleft Palate
Cleft Palate
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases Congenital Abnormality 611 158 0.490 strong 1.000 9 2 2002 2014
CUI: C0008297
Disease: Choanal Atresia
Choanal Atresia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases Congenital Abnormality 104 7 0.410 strong 1.000 2 1 1998 2014
Hypothyroidism, Thyroidal, With Spiky Hair And Cleft Palate
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Endocrine System Diseases; Stomatognathic Diseases Disease or Syndrome 2 1 0.400 None 1.000 1 1 2006 2006
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
disease Neoplasms; Endocrine System Diseases Neoplastic Process 1175 145 0.200 None 1.000 19 4 2001 2020
CUI: C0342200
Disease: Endemic Cretinism
Endemic Cretinism
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases Disease or Syndrome 26 0.200 None 0
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
disease Endocrine System Diseases Disease or Syndrome 613 283 0.150 None 1.000 5 2011 2017
CUI: C0339864
Disease: Bifid epiglottis
Bifid epiglottis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases Congenital Abnormality 8 1 0.120 None 1.000 2 1 2002 2014
CUI: C3501843
Disease: Nonmedullary Thyroid Carcinoma
Nonmedullary Thyroid Carcinoma
disease Neoplasms; Endocrine System Diseases Neoplastic Process 89 3 0.120 None 1.000 2 1 2012 2014
CUI: C0007115
Disease: Malignant neoplasm of thyroid
Malignant neoplasm of thyroid
disease Neoplasms; Endocrine System Diseases Neoplastic Process 949 103 0.100 None 1.000 16 3 2001 2020
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
disease Neoplasms; Endocrine System Diseases Neoplastic Process 1164 135 0.100 None 1.000 16 4 2001 2020
CUI: C1563716
Disease: Thyroid Dysgenesis
Thyroid Dysgenesis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases Congenital Abnormality 24 5 0.100 None 1.000 14 2000 2017
CUI: C1837218
Disease: Cleft palate, isolated
Cleft palate, isolated
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases Congenital Abnormality 295 70 0.100 None 1.000 10 2 2002 2014
Differentiated Thyroid Gland Carcinoma
disease Neoplastic Process 245 80 0.100 None 1.000 10 2 2013 2018
Chronic noninfectious lymphadenopathy
phenotype Hemic and Lymphatic Diseases Finding 12 0.100 None 0
CUI: C3805574
Disease: Increased fracture rate
Increased fracture rate
phenotype Finding 123 0.100 None 0
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability
group Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 2165 159 0.100 None 0
CUI: C4023397
Disease: Abnormal hair quantity
Abnormal hair quantity
disease Anatomical Abnormality 29 0.100 None 0
CUI: C4073245
Disease: Abnormality of neck blood vessel
Abnormality of neck blood vessel
disease Anatomical Abnormality 5 2 0.100 None 0
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
phenotype Finding 473 62 0.100 None 0
CUI: C0206682
Disease: Follicular thyroid carcinoma
Follicular thyroid carcinoma
disease Neoplasms Neoplastic Process 293 28 0.100 None 0