Homer

Gene HMID	Gene Symbol	Organ Specificity	DiseaseID	Disease Name	Related Organ
HM00187	TCHH	pharynx	MESH:D008106	Liver Cirrhosis, Experimental
HM00187	TCHH	pharynx	MESH:D019282	Wasting Syndrome
HM00187	TCHH	pharynx	MESH:D006470	Hemorrhage
HM00187	TCHH	pharynx	MESH:D000013	Congenital Abnormalities
HM00187	TCHH	pharynx	MESH:D000740	Anemia	bone marrow
HM00187	TCHH	pharynx	MESH:D006332	Cardiomegaly
HM00187	TCHH	pharynx	MESH:D020191	Myoclonic Epilepsies, Progressive	nerve
HM00187	TCHH	pharynx	MESH:D020191	Myoclonic Epilepsies, Progressive	muscle
HM00187	TCHH	pharynx	MESH:D019465	Craniofacial Abnormalities
HM00187	TCHH	pharynx	MESH:D008175	Lung Neoplasms	lung
HM00187	TCHH	pharynx	MESH:D054079	Vascular Malformations
HM00187	TCHH	pharynx	MESH:D007249	Inflammation
HM00187	TCHH	pharynx	MESH:D002277	Carcinoma
HM00187	TCHH	pharynx	MESH:D010190	Pancreatic Neoplasms	pancreas
HM00187	TCHH	pharynx	MESH:D012878	Skin Neoplasms
HM00187	TCHH	pharynx	MESH:D004830	Epilepsy, Tonic-Clonic	muscle
HM00187	TCHH	pharynx	MESH:D011230	Precancerous Conditions
HM00187	TCHH	pharynx	MESH:D001943	Breast Neoplasms	breast
HM00187	TCHH	pharynx	MESH:D018281	Cholangiocarcinoma	liver
HM00187	TCHH	pharynx	MESH:D004362	Drug Toxicity
HM00187	TCHH	pharynx	MESH:D019310	Pseudolymphoma
HM00187	TCHH	pharynx	MESH:D005124	Eye Abnormalities
HM00187	TCHH	pharynx	MESH:D008114	Liver Neoplasms, Experimental
HM00187	TCHH	pharynx	MESH:D004831	Epilepsies, Myoclonic	muscle
HM00187	TCHH	pharynx	MESH:D018248	Adenoma, Liver Cell
HM00187	TCHH	pharynx	MESH:D004421	Dystonia
HM00187	TCHH	pharynx	MESH:D012640	Seizures	muscle
HM00187	TCHH	pharynx	MESH:D017119	Porphyria Cutanea Tarda	skin
HM00187	TCHH	pharynx	MESH:D008107	Liver Diseases	skin
HM00187	TCHH	pharynx	MESH:D008107	Liver Diseases	muscle
HM00187	TCHH	pharynx	MESH:D008107	Liver Diseases	lung
HM00187	TCHH	pharynx	MESH:D008107	Liver Diseases	liver
HM00187	TCHH	pharynx	MESH:D006528	Carcinoma, Hepatocellular	liver
HM00187	TCHH	pharynx	MESH:D003294	Seizures, Febrile
HM00187	TCHH	pharynx	MESH:D004832	Epilepsy, Absence	muscle
HM00187	TCHH	pharynx	MESH:D007569	Jaw Abnormalities
HM00187	TCHH	pharynx	MESH:D015619	Respiratory System Abnormalities
HM00187	TCHH	pharynx	MESH:D017202	Myocardial Ischemia	heart
HM00187	TCHH	pharynx	MESH:D009421	Nervous System Malformations
HM00187	TCHH	pharynx	MESH:D001848	Bone Diseases, Developmental
HM00187	TCHH	pharynx	MESH:D006869	Hydronephrosis	kidney
HM00187	TCHH	pharynx	MESH:D004489	Edema, Cardiac
HM00187	TCHH	pharynx	MESH:D005355	Fibrosis
HM00187	TCHH	pharynx	MESH:D013959	Thyroid Diseases	thyroid
HM00187	TCHH	pharynx	MESH:D001836	Body Weight Changes
HM00187	TCHH	pharynx	MESH:D056486	Drug-Induced Liver Injury
HM00187	TCHH	pharynx	MESH:D010382	Peliosis Hepatis	liver
HM00187	TCHH	pharynx	MESH:D011297	Prenatal Exposure Delayed Effects
HM00187	TCHH	pharynx	MESH:D002493	Central Nervous System Diseases	spinal cord
HM00187	TCHH	pharynx	MESH:D002493	Central Nervous System Diseases	skin
HM00187	TCHH	pharynx	MESH:D002493	Central Nervous System Diseases	nerve
HM00187	TCHH	pharynx	MESH:D002493	Central Nervous System Diseases	muscle
HM00187	TCHH	pharynx	MESH:D002493	Central Nervous System Diseases	eye
HM00187	TCHH	pharynx	MESH:D002493	Central Nervous System Diseases	brain
HM00187	TCHH	pharynx	MESH:D006973	Hypertension	lung
HM00187	TCHH	pharynx	MESH:D006973	Hypertension	heart
HM00187	TCHH	pharynx	MESH:D006973	Hypertension	blood vessel
HM00187	TCHH	pharynx	MESH:D004487	Edema
HM00187	TCHH	pharynx	MESH:D017029	Epilepsy, Complex Partial	muscle
HM00187	TCHH	pharynx	MESH:D006529	Hepatomegaly
HM00187	TCHH	pharynx	MESH:D001778	Blood Coagulation Disorders	bone marrow
HM00187	TCHH	pharynx	MESH:D008113	Liver Neoplasms
HM00187	TCHH	pharynx	MESH:D008113	Liver Neoplasms
HM00187	TCHH	pharynx	MESH:D010018	Osteomalacia	bone
HM00187	TCHH	pharynx	MESH:D005313	Fetal Death
HM00187	TCHH	pharynx	MESH:D000014	Abnormalities, Drug-Induced
HM00187	TCHH	pharynx	MESH:D002972	Cleft Palate
HM00187	TCHH	pharynx	MESH:D004827	Epilepsy	muscle
HM00187	TCHH	pharynx	MESH:D006330	Heart Defects, Congenital
HM00187	TCHH	pharynx	MESH:D003924	Diabetes Mellitus, Type 2	pancreas
HM00187	TCHH	pharynx	MESH:D004828	Epilepsies, Partial	muscle