Homer

Gene HMID	Gene Symbol	Organ Specificity	DiseaseID	Disease Name	Related Organ
HM01121	C5	liver	MESH:D006528	Carcinoma, Hepatocellular	liver
HM01121	C5	liver	MESH:D017202	Myocardial Ischemia	heart
HM01121	C5	liver	MESH:D001943	Breast Neoplasms	breast
HM01121	C5	liver	MESH:D006332	Cardiomegaly
HM01121	C5	liver	MESH:D011565	Psoriasis	skin
HM01121	C5	liver	MESH:D013959	Thyroid Diseases	thyroid
HM01121	C5	liver	MESH:D009404	Nephrotic Syndrome	kidney
HM01121	C5	liver	MESH:D008106	Liver Cirrhosis, Experimental
HM01121	C5	liver	OMIM:609536	COMPLEMENT COMPONENT 5 DEFICIENCY
HM01121	C5	liver	MESH:D006869	Hydronephrosis	kidney
HM01121	C5	liver	MESH:D014985	Xerophthalmia	eye
HM01121	C5	liver	MESH:D005885	Gingival Hyperplasia
HM01121	C5	liver	MESH:D007569	Jaw Abnormalities
HM01121	C5	liver	MESH:D009402	Nephrosis, Lipoid	kidney
HM01121	C5	liver	MESH:D008664	Metal Metabolism, Inborn Errors	skin
HM01121	C5	liver	MESH:D008664	Metal Metabolism, Inborn Errors	muscle
HM01121	C5	liver	MESH:D008664	Metal Metabolism, Inborn Errors	liver
HM01121	C5	liver	MESH:D008664	Metal Metabolism, Inborn Errors	kidney
HM01121	C5	liver	MESH:D015619	Respiratory System Abnormalities
HM01121	C5	liver	MESH:D000014	Abnormalities, Drug-Induced
HM01121	C5	liver	MESH:D018281	Cholangiocarcinoma	liver
HM01121	C5	liver	MESH:D001778	Blood Coagulation Disorders	bone marrow
HM01121	C5	liver	MESH:D010382	Peliosis Hepatis	liver
HM01121	C5	liver	MESH:D001836	Body Weight Changes
HM01121	C5	liver	MESH:D006330	Heart Defects, Congenital
HM01121	C5	liver	MESH:D006984	Hypertrophy
HM01121	C5	liver	MESH:D054079	Vascular Malformations
HM01121	C5	liver	MESH:D012852	Sinusitis
HM01121	C5	liver	MESH:D012878	Skin Neoplasms
HM01121	C5	liver	MESH:D056486	Drug-Induced Liver Injury
HM01121	C5	liver	MESH:D005124	Eye Abnormalities
HM01121	C5	liver	MESH:D007674	Kidney Diseases	ureter
HM01121	C5	liver	MESH:D007674	Kidney Diseases	pituitary
HM01121	C5	liver	MESH:D007674	Kidney Diseases	kidney
HM01121	C5	liver	MESH:D004489	Edema, Cardiac
HM01121	C5	liver	MESH:D000740	Anemia	bone marrow
HM01121	C5	liver	MESH:D007105	Immune Complex Diseases	skin
HM01121	C5	liver	MESH:D007105	Immune Complex Diseases	bone marrow
HM01121	C5	liver	MESH:D000013	Congenital Abnormalities
HM01121	C5	liver	MESH:D007638	Keratoconjunctivitis Sicca	eye
HM01121	C5	liver	MESH:D001848	Bone Diseases, Developmental
HM01121	C5	liver	MESH:D005355	Fibrosis
HM01121	C5	liver	MESH:D008175	Lung Neoplasms	lung
HM01121	C5	liver	MESH:D006470	Hemorrhage
HM01121	C5	liver	MESH:D005313	Fetal Death
HM01121	C5	liver	MESH:D008113	Liver Neoplasms
HM01121	C5	liver	MESH:D008113	Liver Neoplasms
HM01121	C5	liver	MESH:D019846	Miller Fisher Syndrome	bone marrow
HM01121	C5	liver	MESH:D006973	Hypertension	lung
HM01121	C5	liver	MESH:D006973	Hypertension	heart
HM01121	C5	liver	MESH:D006973	Hypertension	blood vessel
HM01121	C5	liver	MESH:D004362	Drug Toxicity
HM01121	C5	liver	MESH:D019465	Craniofacial Abnormalities
HM01121	C5	liver	MESH:D004487	Edema
HM01121	C5	liver	MESH:D018248	Adenoma, Liver Cell
HM01121	C5	liver	MESH:D006457	Hemoglobinuria, Paroxysmal
HM01121	C5	liver	MESH:D006529	Hepatomegaly
HM01121	C5	liver	MESH:D008114	Liver Neoplasms, Experimental
HM01121	C5	liver	MESH:D014605	Uveitis	eye
HM01121	C5	liver	MESH:D002972	Cleft Palate
HM01121	C5	liver	MESH:D007249	Inflammation
HM01121	C5	liver	MESH:D020720	Myasthenia Gravis, Autoimmune, Experimental
HM01121	C5	liver	MESH:D009421	Nervous System Malformations
HM01121	C5	liver	MESH:D017119	Porphyria Cutanea Tarda	skin
HM01121	C5	liver	MESH:D007948	Leukemia, Monocytic, Acute	bone marrow
HM01121	C5	liver	MESH:D001145	Arrhythmias, Cardiac
HM01121	C5	liver	MESH:D011297	Prenatal Exposure Delayed Effects
HM01121	C5	liver	MESH:D002277	Carcinoma
HM01121	C5	liver	MESH:D003924	Diabetes Mellitus, Type 2	pancreas
HM01121	C5	liver	MESH:D001919	Bradycardia
HM01121	C5	liver	MESH:D019282	Wasting Syndrome

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