Homer

Gene HMID	Gene Symbol	Organ Specificity	DiseaseID	Disease Name	Related Organ
HM04863	STON1	blood vessel	MESH:D017114	Liver Failure, Acute
HM04863	STON1	blood vessel	MESH:D008106	Liver Cirrhosis, Experimental
HM04863	STON1	blood vessel	MESH:D004831	Epilepsies, Myoclonic	muscle
HM04863	STON1	blood vessel	MESH:D017029	Epilepsy, Complex Partial	muscle
HM04863	STON1	blood vessel	MESH:D001008	Anxiety Disorders
HM04863	STON1	blood vessel	MESH:D016135	Spinal Dysraphism	spinal cord
HM04863	STON1	blood vessel	MESH:D014178	Translocation, Genetic
HM04863	STON1	blood vessel	MESH:D006849	Hydrocephalus	brain
HM04863	STON1	blood vessel	MESH:D012208	Rhabdomyosarcoma	rectum
HM04863	STON1	blood vessel	MESH:D012208	Rhabdomyosarcoma	prostate
HM04863	STON1	blood vessel	MESH:D012208	Rhabdomyosarcoma	muscle
HM04863	STON1	blood vessel	MESH:D000015	Abnormalities, Multiple
HM04863	STON1	blood vessel	MESH:D020194	Unverricht-Lundborg Syndrome	muscle
HM04863	STON1	blood vessel	MESH:D005315	Fetal Diseases
HM04863	STON1	blood vessel	MESH:D004421	Dystonia
HM04863	STON1	blood vessel	MESH:D006932	Hyperbilirubinemia
HM04863	STON1	blood vessel	MESH:D012640	Seizures	muscle
HM04863	STON1	blood vessel	MESH:D001714	Bipolar Disorder
HM04863	STON1	blood vessel	MESH:D009190	Myelodysplastic Syndromes
HM04863	STON1	blood vessel	MESH:D000014	Abnormalities, Drug-Induced
HM04863	STON1	blood vessel	MESH:D013226	Status Epilepticus	muscle
HM04863	STON1	blood vessel	MESH:D013226	Status Epilepticus	muscle
HM04863	STON1	blood vessel	MESH:D013226	Status Epilepticus	muscle
HM04863	STON1	blood vessel	MESH:D008103	Liver Cirrhosis	liver
HM04863	STON1	blood vessel	MESH:D014564	Urogenital Abnormalities
HM04863	STON1	blood vessel	MESH:D009139	Musculoskeletal Abnormalities
HM04863	STON1	blood vessel	MESH:D056486	Drug-Induced Liver Injury
HM04863	STON1	blood vessel	MESH:D004827	Epilepsy	muscle
HM04863	STON1	blood vessel	MESH:D001321	Autistic Disorder
HM04863	STON1	blood vessel	MESH:D006505	Hepatitis
HM04863	STON1	blood vessel	MESH:D005355	Fibrosis
HM04863	STON1	blood vessel	MESH:D001848	Bone Diseases, Developmental
HM04863	STON1	blood vessel	MESH:D004832	Epilepsy, Absence	muscle
HM04863	STON1	blood vessel	MESH:D002252	Carbon Tetrachloride Poisoning
HM04863	STON1	blood vessel	MESH:D004828	Epilepsies, Partial	muscle
HM04863	STON1	blood vessel	MESH:D005317	Fetal Growth Retardation
HM04863	STON1	blood vessel	MESH:D019465	Craniofacial Abnormalities
HM04863	STON1	blood vessel	MESH:D005234	Fatty Liver
HM04863	STON1	blood vessel	MESH:D019310	Pseudolymphoma
HM04863	STON1	blood vessel	MESH:D017563	Lung Diseases, Interstitial	lung
HM04863	STON1	blood vessel	MESH:D000550	Amblyopia	brain
HM04863	STON1	blood vessel	MESH:D000550	Amblyopia	brain
HM04863	STON1	blood vessel	MESH:D004830	Epilepsy, Tonic-Clonic	muscle
HM04863	STON1	blood vessel	MESH:D008114	Liver Neoplasms, Experimental
HM04863	STON1	blood vessel	MESH:D009436	Neural Tube Defects
HM04863	STON1	blood vessel	MESH:D012559	Schizophrenia
HM04863	STON1	blood vessel	MESH:D017093	Liver Failure
HM04863	STON1	blood vessel	MESH:D015470	Leukemia, Myeloid, Acute	bone marrow
HM04863	STON1	blood vessel	MESH:D008107	Liver Diseases	skin
HM04863	STON1	blood vessel	MESH:D008107	Liver Diseases	muscle
HM04863	STON1	blood vessel	MESH:D008107	Liver Diseases	lung
HM04863	STON1	blood vessel	MESH:D008107	Liver Diseases	liver
HM04863	STON1	blood vessel	MESH:D008881	Migraine Disorders	brain

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