C4A, complement C4A (Rodgers blood group), 720

N. diseases: 145; N. variants: 2
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: C3280742
Disease: SYSTEMIC LUPUS ERYTHEMATOSUS 16
SYSTEMIC LUPUS ERYTHEMATOSUS 16 		disease Disease or Syndrome 5 0.300 None 1.000 1 2004 2004
CUI: C3899844
Disease: C4 Deficiency
C4 Deficiency 		disease Disease or Syndrome 5 0.010 None 1.000 1 1998 1998
CUI: C3280642
Disease: Complement Component 4a Deficiency
Complement Component 4a Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases Disease or Syndrome 6 0.550 strong 1.000 6 1990 2016
CUI: C3280641
Disease: Decreased serum complement C4b
Decreased serum complement C4b 		disease Disease or Syndrome 8 0.010 None 1.000 1 2010 2010
CUI: C3150275
Disease: COMPLEMENT COMPONENT 2 DEFICIENCY
COMPLEMENT COMPONENT 2 DEFICIENCY 		disease Disease or Syndrome 11 4 0.010 None 1.000 1 1992 1992
CUI: C0237653
Disease: Immunologic hypersensitivity
Immunologic hypersensitivity 		phenotype Pathologic Function 16 0.100 None 0
CUI: C0343084
Disease: Capillary Leak Syndrome
Capillary Leak Syndrome 		disease Cardiovascular Diseases Disease or Syndrome 18 0.010 None 1.000 1 2004 2004
CUI: C0085582
Disease: Retrobulbar Neuritis
Retrobulbar Neuritis 		disease Eye Diseases; Nervous System Diseases Disease or Syndrome 18 0.100 None 0
CUI: C4025758
Disease: Abnormal myocardium morphology
Abnormal myocardium morphology 		phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Anatomical Abnormality 19 0.100 None 0
CUI: C0003257
Disease: Antibody Deficiency Syndrome
Antibody Deficiency Syndrome 		disease Immune System Diseases Disease or Syndrome 21 0.300 None 1.000 1 1993 1993
CUI: C0409979
Disease: Neonatal Systemic lupus erythematosus
Neonatal Systemic lupus erythematosus 		disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 22 1 0.010 None 1.000 1 1992 1992
CUI: C0029191
Disease: Orchitis
Orchitis 		phenotype Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 30 0.100 None 0
CUI: C0151942
Disease: Arterial thrombosis
Arterial thrombosis 		phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 33 1 0.100 None 0
CUI: C0024140
Disease: Lupus Erythematosus, Subacute Cutaneous
Lupus Erythematosus, Subacute Cutaneous 		disease Skin and Connective Tissue Diseases Disease or Syndrome 39 1 0.010 None 1.000 1 1993 1993
CUI: C0085660
Disease: Aseptic necrosis
Aseptic necrosis 		phenotype Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Pathologic Function 41 0.100 None 0
CUI: C3887513
Disease: Avascular necrosis
Avascular necrosis 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 41 0.100 None 0
CUI: C4553018
Disease: Avascular Necrosis, CTCAE
Avascular Necrosis, CTCAE 		phenotype Finding 41 0.100 None 0
CUI: C0272242
Disease: Complement deficiency disease
Complement deficiency disease 		group Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 42 0.400 strong 1.000 1 2011 2011
CUI: C0235896
Disease: Pulmonary Infiltrate
Pulmonary Infiltrate 		phenotype Respiratory Tract Diseases Finding 43 0.100 None 0
CUI: C2936858
Disease: Congenital adrenal hyperplasia due to 21 hydroxylase deficiency
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Congenital Abnormality 50 62 0.020 None 1.000 2 1986 1986
CUI: C0031046
Disease: Pericarditis
Pericarditis 		disease Cardiovascular Diseases Disease or Syndrome 51 6 0.100 None 0
CUI: C0221023
Disease: Cyclic neutropenia
Cyclic neutropenia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 52 14 0.010 None 1.000 1 1985 1985
CUI: C0403447
Disease: Chronic Kidney Insufficiency
Chronic Kidney Insufficiency 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 52 12 0.010 None 1.000 1 1991 1991
CUI: C0042165
Disease: Anterior uveitis
Anterior uveitis 		disease Eye Diseases Disease or Syndrome 53 20 0.010 None 1.000 1 1988 1988
CUI: C0268287
Disease: Deficiency of steroid 21-monooxygenase
Deficiency of steroid 21-monooxygenase 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Congenital Abnormality 54 26 0.010 None 1.000 1 1986 1986