Homer logoHomer

Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM05559FAM184Alymph nodeMESH:D000550Amblyopiabrain
HM05559FAM184Alymph nodeMESH:D000550Amblyopiabrain
HM05559FAM184Alymph nodeMESH:D019465Craniofacial Abnormalities
HM05559FAM184Alymph nodeMESH:D020194Unverricht-Lundborg Syndromemuscle
HM05559FAM184Alymph nodeMESH:D005234Fatty Liver
HM05559FAM184Alymph nodeMESH:D004827Epilepsymuscle
HM05559FAM184Alymph nodeMESH:D001848Bone Diseases, Developmental
HM05559FAM184Alymph nodeMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM05559FAM184Alymph nodeMESH:D009139Musculoskeletal Abnormalities
HM05559FAM184Alymph nodeMESH:D001321Autistic Disorder
HM05559FAM184Alymph nodeMESH:D019310Pseudolymphoma
HM05559FAM184Alymph nodeMESH:D001008Anxiety Disorders
HM05559FAM184Alymph nodeMESH:D012640Seizuresmuscle
HM05559FAM184Alymph nodeMESH:D008881Migraine Disordersbrain
HM05559FAM184Alymph nodeMESH:D012559Schizophrenia
HM05559FAM184Alymph nodeMESH:D016135Spinal Dysraphismspinal cord
HM05559FAM184Alymph nodeMESH:D014564Urogenital Abnormalities
HM05559FAM184Alymph nodeMESH:D004832Epilepsy, Absencemuscle
HM05559FAM184Alymph nodeMESH:D006849Hydrocephalusbrain
HM05559FAM184Alymph nodeMESH:D004421Dystonia
HM05559FAM184Alymph nodeMESH:D017029Epilepsy, Complex Partialmuscle
HM05559FAM184Alymph nodeMESH:D005317Fetal Growth Retardation
HM05559FAM184Alymph nodeMESH:D013226Status Epilepticusmuscle
HM05559FAM184Alymph nodeMESH:D013226Status Epilepticusmuscle
HM05559FAM184Alymph nodeMESH:D013226Status Epilepticusmuscle
HM05559FAM184Alymph nodeMESH:D005315Fetal Diseases
HM05559FAM184Alymph nodeMESH:D004831Epilepsies, Myoclonicmuscle
HM05559FAM184Alymph nodeMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM05559FAM184Alymph nodeMESH:D012208Rhabdomyosarcomarectum
HM05559FAM184Alymph nodeMESH:D012208Rhabdomyosarcomaprostate
HM05559FAM184Alymph nodeMESH:D012208Rhabdomyosarcomamuscle
HM05559FAM184Alymph nodeMESH:D017563Lung Diseases, Interstitiallung
HM05559FAM184Alymph nodeMESH:D000015Abnormalities, Multiple
HM05559FAM184Alymph nodeMESH:D001714Bipolar Disorder
HM05559FAM184Alymph nodeMESH:D000014Abnormalities, Drug-Induced
HM05559FAM184Alymph nodeMESH:D056486Drug-Induced Liver Injury
HM05559FAM184Alymph nodeMESH:D009190Myelodysplastic Syndromes
HM05559FAM184Alymph nodeMESH:D009436Neural Tube Defects
HM05559FAM184Alymph nodeMESH:D004828Epilepsies, Partialmuscle
HM05559FAM184Alymph nodeMESH:D014178Translocation, Genetic