SERPINA7, serpin family A member 7, 6906

N. diseases: 51; N. variants: 6
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: C0025521
Disease: Inborn Errors of Metabolism
Inborn Errors of Metabolism 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome; Congenital Abnormality 119 3 0.300 None 1.000 1 1990 1990
CUI: C0023893
Disease: Liver Cirrhosis, Experimental
Liver Cirrhosis, Experimental 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Experimental Model of Disease 870 0.300 None 1.000 1 2014 2014
CUI: C0020550
Disease: Hyperthyroidism
Hyperthyroidism 		disease Endocrine System Diseases Disease or Syndrome 279 27 0.220 None 1.000 3 1976 2019
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		disease Endocrine System Diseases Disease or Syndrome 613 283 0.210 None 1.000 1 1990 1990
CUI: C3711378
Disease: Inherited Thyroxine-Binding Globulin Deficiency
Inherited Thyroxine-Binding Globulin Deficiency 		disease Endocrine System Diseases Disease or Syndrome 2 2 0.100 None 1.000 12 1 1976 2019
CUI: C3890934
Disease: THYROXINE-BINDING GLOBULIN, VARIANT P PHENOTYPE
THYROXINE-BINDING GLOBULIN, VARIANT P PHENOTYPE 		phenotype Finding 1 1 0.100 None 0 1
CUI: C4016583
Disease: THYROXINE-BINDING GLOBULIN, SLOW
THYROXINE-BINDING GLOBULIN, SLOW 		phenotype Finding 1 1 0.100 None 0 1
CUI: C3890933
Disease: THYROXINE-BINDING GLOBULIN, VARIANT A PHENOTYPE
THYROXINE-BINDING GLOBULIN, VARIANT A PHENOTYPE 		phenotype Finding 1 1 0.100 None 0 1
CUI: C4016587
Disease: THYROXINE-BINDING GLOBULIN, CHICAGO
THYROXINE-BINDING GLOBULIN, CHICAGO 		phenotype Finding 1 1 0.100 None 0 1
CUI: C0271836
Disease: X-linked reduction of thyroxine-binding globulin
X-linked reduction of thyroxine-binding globulin 		disease Disease or Syndrome 1 1 0.100 None 0 1
CUI: C0342185
Disease: Hyperthyroxinemia, Familial Dysalbuminemic
Hyperthyroxinemia, Familial Dysalbuminemic 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases Disease or Syndrome 12 4 0.060 None 1.000 6 1987 2004
CUI: C1839141
Disease: Thyroxine-Binding Globulin Deficiency
Thyroxine-Binding Globulin Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 3 2 0.050 None 1.000 5 1994 2019
CUI: C0027651
Disease: Neoplasms
Neoplasms 		group Neoplasms Neoplastic Process 10161 1644 0.020 None 1.000 2 1992 2017
CUI: C0040156
Disease: Thyrotoxicosis
Thyrotoxicosis 		disease Endocrine System Diseases Disease or Syndrome 37 7 0.020 None 1.000 2 1976 1988
CUI: C0206624
Disease: Hepatoblastoma
Hepatoblastoma 		disease Neoplasms Neoplastic Process 452 22 0.020 None 1.000 2 1992 1993
CUI: C0342881
Disease: Familial hypercholesterolemia - homozygous
Familial hypercholesterolemia - homozygous 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 23 72 0.020 None 1.000 2 2017 2017
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		disease Digestive System Diseases; Neoplasms Neoplastic Process 5725 942 0.020 None 0.500 2 1984 1988
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		group Cardiovascular Diseases Disease or Syndrome 2322 1085 0.020 None 1.000 2 2016 2017
CUI: C0349486
Disease: Transient hypothyroxinemia
Transient hypothyroxinemia 		disease Endocrine System Diseases Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C4329989
Disease: Feline Oral Squamous Cell Carcinoma
Feline Oral Squamous Cell Carcinoma 		disease Neoplastic Process 3 0.010 None 1.000 1 2017 2017
CUI: C4302200
Disease: Congenital central hypothyroidism
Congenital central hypothyroidism 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases Disease or Syndrome 8 0.010 None 1.000 1 2017 2017
CUI: C0520463
Disease: Chronic active hepatitis
Chronic active hepatitis 		disease Digestive System Diseases Disease or Syndrome 122 34 0.010 None 1.000 1 1988 1988
CUI: C0677886
Disease: Epithelial ovarian cancer
Epithelial ovarian cancer 		disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Neoplastic Process 1224 129 0.010 None 1.000 1 2015 2015
CUI: C0744620
Disease: Metastatic Head and Neck Squamous Cell Carcinoma
Metastatic Head and Neck Squamous Cell Carcinoma 		disease Neoplasms Neoplastic Process 17 0.010 None 1.000 1 2014 2014
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
Squamous cell carcinoma of the head and neck 		disease Neoplasms Neoplastic Process 1543 348 0.010 None < 0.001 1 2014 2014