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monarch-initiative / monarch-disease-ontology-RETIRED

THIS IS THE OLD REPO: Use this one instead: https://github.com/monarch-initiative/mondo-build
https://github.com/monarch-initiative/mondo-build
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High-level disease groupings don't seem to be consistent, intuitive #235

Closed jmcmurry closed 6 years ago

jmcmurry commented 7 years ago

I was looking to show off MONDO browsing in the website, but am a bit hesitant because the highest-level groupings seem a bit too granular, inconsistent. Thoughts? @cmungall

https://monarchinitiative.org/disease/DOID:4 [subClassOf] 17-Hydroxysteroid Dehydrogenase Deficiency [subClassOf] 46,XX Sex Reversal [subClassOf] Acetylation, Slow [subClassOf] Activator Of Liver Function 1 [subClassOf] Acute Insulin Response [subClassOf] Acyl-Coa Thioester Hydrolase, Long-Chain, 1 [subClassOf] Acylase, Cobalt-Activated [subClassOf] Adrenal Hyperplasia [subClassOf] Adrenal Hypoplasia [subClassOf] Age-Related Hearing Impairment [subClassOf] Anosmia [subClassOf] Antigen Defined By Monoclonal Antibody Aj9 [subClassOf] Antigen Defined By Monoclonal Antibody T87 [subClassOf] Antipyrine Metabolism [subClassOf] Antiviral State Repressor, Regulator Of [subClassOf] Apnea [subClassOf] Arbitrary Restriction Polymorphism 1 [subClassOf] Aspirin Resistance [subClassOf] Ataxia-Oculomotor Apraxia [subClassOf] Ataxia-Telangiectasia-Like Disorder [subClassOf] Atrial Standstill [subClassOf] Atypical Mycobacteriosis, Familial [subClassOf] Autoimmune Disease, Multisystem, Infantile-Onset [subClassOf] Autoinflammatory Syndrome, Familial, Behcet-Like; AISBL [subClassOf] B-Cell Growth Factor [subClassOf] BPH [subClassOf] Bacteremia, Susceptibility [subClassOf] Bare Lymphocyte Syndrome [subClassOf] Bifid Nose [subClassOf] Biological Anomaly Without Phenotypic Characterization [subClassOf] Body Length, Mouse, Human Homolog [subClassOf] Bombay Phenotype [subClassOf] Bone Marrow Failure Syndrome [subClassOf] Butyrylesterase 1 [subClassOf] Camptodactyly Syndrome, Guadalajara [subClassOf] Camptodactyly, Myopia, And Fibrosis Of The Medial Rectus Muscle Of Eye [subClassOf] Carbimazole Sensitivity [subClassOf] Caronte [subClassOf] Cd4/Cd8 T-Cell Ratio [subClassOf] Cerebellar Atrophy, Visual Impairment, And Psychomotor Retardation; [subClassOf] Cerebelloparenchymal Disorder [subClassOf] Cerebral Arteriopathy, Autosomal Dominant, With Subcortical Infarcts And Leukoencephalopathy; CADASIL [subClassOf] Cerebral Cavernous Malformations [subClassOf] Cerebral Malformation, Seizures, Hypertrichosis, And Overlapping Fingers [subClassOf] Chiari Malformation [subClassOf] Chlorpropamide-Alcohol Flushing [subClassOf] Chondrodysplasia [subClassOf] Chondronectin [subClassOf] Chorea, Childhood-Onset, With Psychomotor Retardation; COCPMR [subClassOf] Choreoathetosis [subClassOf] Chromosome 16 Inversion, 0.45-Mb [subClassOf] Chronic Mountain Sickness, Susceptibility To [subClassOf] Cleft Palate, Psychomotor Retardation, And Distinctive Facial Features; [subClassOf] Colchicine Resistance [subClassOf] Coronary Heart Disease [subClassOf] Corpus Callosum, Agenesis Of, With Facial Anomalies And Cerebellar Ataxia; CCAFCA [subClassOf] Corticosterone Methyloxidase Deficiency [subClassOf] Cortisone Reductase Deficiency [subClassOf] Cyanosis, Transient Neonatal [subClassOf] Dauwerse-Peters Syndrome [subClassOf] Dehydrated Hereditary Stomatocytosis [subClassOf] Dengue Virus, Susceptibility To [subClassOf] Developmental Delay With Short Stature, Dysmorphic Features, And Sparse Hair; DEDSSH [subClassOf] Developmental Dysplasia Of The Hip [subClassOf] Disorganization, Mouse, Homolog Of [subClassOf] Dna, Low-Repetitive Sequences Of [subClassOf] Dna, Satellite, 3 [subClassOf] Dna, Satellite, Alpha Type [subClassOf] Dopamine Beta-Hydroxylase, Plasma, Thermolability Of [subClassOf] Dwarfism, Mental Retardation, And Eye Abnormality [subClassOf] Dyskinesia, Limb And Orofacial, Infantile-Onset; IOLOD [subClassOf] Early Repolarization Associated With Ventricular Fibrillation [subClassOf] Early Response To Neural Induction Gene [subClassOf] Ectodermal Dysplasia [subClassOf] Ectopia Lentis, Isolated [subClassOf] Eculizumab, Poor Response To [subClassOf] Efavirenz, Poor Metabolism Of [subClassOf] Egasyn [subClassOf] Emphysema [subClassOf] Enolase, Sperm Specific [subClassOf] Enuresis, Nocturnal [subClassOf] Epidermolysis Bullosa Simplex With Nail Dystrophy [subClassOf] Epilepsy, Hearing Loss, And Mental Retardation Syndrome [subClassOf] Epileptic Encephalopathy, Early Infantile, 38; EIEE38 [subClassOf] Episodic Pain Syndrome, Familial [subClassOf] Epithelial Basolateral Chloride Conductance Regulator, Rabbit, Homolog Of [subClassOf] Esterase B [subClassOf] Esterase C [subClassOf] Esterase Es-2, Regulator For [subClassOf] Eukaryotic Translation Elongation Factor 1 Alpha-1-Like 14 [subClassOf] Even-Plus Syndrome; EVPLS [subClassOf] Exercise Intolerance, Riboflavin-Responsive; RREI [subClassOf] Exostosis, Dupuytren Subungual [subClassOf] FRAXF Syndrome [subClassOf] Facial Paresis, Hereditary Congenital [subClassOf] Factor V And Factor VIII, Combined Deficiency Of [subClassOf] Famailial Adenomatous Polyposis [subClassOf] Familial Cold Autoinflammatory Syndrome [subClassOf] Febrile Seizures, Familial [subClassOf] Focal Facial Dermal Dysplasia [subClassOf] Folate Level 1N Erythrocytes [subClassOf] Fragile Site 10Q23 [subClassOf] Frontonasal Dysplasia [subClassOf] Fructose Utilization [subClassOf] Fucosidase Regulator [subClassOf] GLUT1 Deficiency Syndrome [subClassOf] Gastric Cancer [subClassOf] Gastric Juice Peptides [subClassOf] Geleophysic Dysplasia [subClassOf] Glomerulopathy With Fibronectin Deposits [subClassOf] Glucocorticoid Deficiency [subClassOf] Glucocorticoid Therapy, Response To [subClassOf] Glutamic Acid Decarboxylase, Brain, Membrane Form [subClassOf] Glutaric Aciduria [subClassOf] Glutathione Transferase Activity Toward Trans-Stilbene Oxide [subClassOf] Glycoprotein, Renal [subClassOf] Griscelli Syndrome [subClassOf] Growth Restriction, Severe, With Distinctive Facies [subClassOf] Guanylate Cyclase 2E [subClassOf] Guanylate Kinase 3 [subClassOf] Halo Nevi [subClassOf] Hand Clasping Pattern [subClassOf] Heart And Brain Malformation Syndrome; HBMS [subClassOf] Heat-Shock Rna 1 [subClassOf] Heimler Syndrome [subClassOf] Hematopoietic Stem Cell Kinetics, Control Of [subClassOf] Hla Modifier [subClassOf] Horns 1N Sheep [subClassOf] Hpa 1 Recognition Polymorphism, Beta-Globin-Related [subClassOf] Huntington Disease-Like [subClassOf] Hydrops, Lactic Acidosis, And Sideroblastic Anemia; HLASA [subClassOf] Hyperaldosteronism, Familial, Type IV; HALD4 [subClassOf] Hypercalcemia, Infantile [subClassOf] Hypercalciuria, Absorptive [subClassOf] Hyperekplexia [subClassOf] Hypermanganesemia With Dystonia [subClassOf] Hyperphosphatasia With Mental Retardation Syndrome [subClassOf] Hyperpigmentation, Familial Progressive [subClassOf] Hyperprolinemia [subClassOf] Hypervitaminosis A, Susceptibility To [subClassOf] Hypocalcemia [subClassOf] Hypomagnesemia [subClassOf] Hypophosphatemic Rickets [subClassOf] Hypotonia, Infantile, With Psychomotor Retardation And Characteristic Facies [subClassOf] Hypotonia, Infantile, With Psychomotor Retardation; IHPMR [subClassOf] Hypouricemia, Renal [subClassOf] Hypoxanthine Guanine Phosphoribosyltransferase Suppressor [subClassOf] Immunoglobulin A Deficiency [subClassOf] Immunoglobulin Switch Sequences [subClassOf] Imprinting Gene Related To Retinoblastoma [subClassOf] Interferon Antiviral Depressor [subClassOf] Invasive Pneumococcal Disease, Recurrent Isolated [subClassOf] Iris Pattern [subClassOf] Isolated Growth Hormone Deficiency [subClassOf] Isoproterenol-Mediated Vasodilatation [subClassOf] Keratoderma, Palmoplantar, With Nail Dystrophy And Hereditary Motor-Sensory Neuropathy [subClassOf] Keratosis Pilaris [subClassOf] Kosaki Overgrowth Syndrome [subClassOf] Lethal Congenital Contracture Syndrome 10; LCCS10 [subClassOf] Leukodystrophy And Acquired Microcephaly With Or Without Dystonia; [subClassOf] Leukoregulin [subClassOf] Linear Skin Defects With Multiple Congenital Anomalies [subClassOf] Lipoprotein Types--Lt System [subClassOf] Lipoprotein, Variant Of Beta [subClassOf] Long Chain Fatty Acids, Defect 1N Transport Of [subClassOf] Low Density Lipoprotein Cholesterol, Mild Elevation Of [subClassOf] Low Density Lipoprotein, Variation 1N Molecular Weight Of [subClassOf] Luscan-Lumish Syndrome; LLS [subClassOf] Lymphoproliferative Syndrome [subClassOf] MSPC [subClassOf] Macrocephaly, Dysmorphic Facies, And Psychomotor Retardation; MDFPMR [subClassOf] Macular Degeneration, Early-Onset [subClassOf] Macular Dystrophy [subClassOf] Magnesium, Elevated Red Cell [subClassOf] Malposition Of Teeth With Or Without Hypodontia/Oligodontia [subClassOf] Mammastatin [subClassOf] Mcleod Syndrome [subClassOf] Medullary Cystic Kidney Disease [subClassOf] Megarbane-Jalkh Syndrome [subClassOf] Melanoma Tumor Antigen Gp90 [subClassOf] Melanoma, Cutaneous Malignant [subClassOf] Mental Retardation, X-Linked, Nonsyndromic [subClassOf] Mesoaxial Hexadactyly And Cardiac Malformation [subClassOf] Metabolic Encephalomyopathic Crises, Recurrent, With Rhabdomyolysis, Cardiac Arrhythmias, And Neurodegeneration; MECRCN [subClassOf] Metachromasia Of Fibroblasts [subClassOf] Metaphyseal Modeling Abnormality, Skin Lesions, And Spastic Paraplegia [subClassOf] Microcephalic Primordial Dwarfism [subClassOf] Microcephaly, Congenital Cataract, And Psoriasiform Dermatitis; MCCPD [subClassOf] Microcephaly, Primary, Autosomal Recessive [subClassOf] Microcephaly, Short Stature, And Impaired Glucose Metabolism [subClassOf] Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma [subClassOf] Mirage Syndrome; MIRAGE [subClassOf] Mitochondrial Complex Deficiency [subClassOf] Mitochondrial DNA Depletion Syndrome [subClassOf] Mitochondrial Import-Stimulating Factor [subClassOf] Mitochondrial Intermembrane Space Protein Tim12, Yeast, Homolog Of [subClassOf] Molybdenum Cofactor Deficiency [subClassOf] Mosaic Variegated Aneuploidy Syndrome [subClassOf] Mucolipidosis [subClassOf] Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome [subClassOf] Multiple Endocrine Neoplasia [subClassOf] Multiple Mitochondrial Dysfunctions Syndrome [subClassOf] Mutagen Sensitivity [subClassOf] Myelolymphatic Insufficiency [subClassOf] Myeloproliferative/Lymphoproliferative Neoplasms, Familial (Multiple Types), Susceptibility To; MPLPF [subClassOf] Myoclonus And Ataxia [subClassOf] Myopathy, Isolated Mitochondrial, Autosomal Dominant [subClassOf] Myopathy, Myofibrillar [subClassOf] Myostatin-Related Muscle Hypertrophy [subClassOf] NAD [subClassOf] NM [subClassOf] Nail Disorder, Nonsyndromic Congenital [subClassOf] Nerve Growth Factor, Alpha Subunit [subClassOf] Neu-Laxova Syndrome [subClassOf] Neurodegeneration With Brain Iron Accumulation [subClassOf] Neurodevelopmental Disorder With Or Without Anomalies Of The Brain, Eye, Or Heart; NEDBEH [subClassOf] Neuropathy, Hereditary Sensory And Autonomic [subClassOf] Nevus Comedonicus; NC [subClassOf] Nuclear Ribonucleic Acid [subClassOf] Nystagmus [subClassOf] Occipital Hair, White Lock Of [subClassOf] Ocular Cicatricial Pemphigoid [subClassOf] Ocular Dominance [subClassOf] Oculocerebral Hypopigmentation Syndrome Of Preus [subClassOf] Okt4 Epitope Deficiency [subClassOf] Oncocytoma [subClassOf] Oncogene Yuasa [subClassOf] Oocyte Maturation Defect; OOMD [subClassOf] Optic Atrophy, Hearing Loss, And Peripheral Neuropathy, Autosomal Recessive [subClassOf] Oral Sensibility, Disturbance Of [subClassOf] Osteochondrodysplasia, Complex Lethal, Symoens-Barnes-Gistelinck Type; [subClassOf] Oto-Palato-Digital Syndrome [subClassOf] Otofaciocervical Syndrome [subClassOf] Otoonychoperoneal Syndrome [subClassOf] Ouabain Resistance [subClassOf] Ovarian Dysgenesis [subClassOf] Ovarian Dysgenesis, Hypergonadotropic, With Short Stature And Recurrent Metabolic Acidosis [subClassOf] PCD [subClassOf] PDCOS [subClassOf] PDDP [subClassOf] Pa Polymorphism Of Alpha-2-Globulin [subClassOf] Pectus Excavatum, Macrocephaly, Short Stature, And Dysplastic Nails [subClassOf] Pelvic Organ Prolapse [subClassOf] Pepsinogen 3, Group 1 [subClassOf] Peripartum Cardiomyopathy, Susceptibility To [subClassOf] Peroneus Tertius Muscle, Absence Of [subClassOf] Peroxidase, Salivary [subClassOf] Phenformin 4-Hydroxylation [subClassOf] Phosphatase, Acid, Of Tissues [subClassOf] Phosphoglucomutase 4 [subClassOf] Phosphoglycoprotein 1 [subClassOf] Phosphohydroxylysinuria [subClassOf] Pituitary Hormone Deficiency, Combined [subClassOf] Plasma Fibronectin Deficiency [subClassOf] Platelet Adenylate Cyclase Activity [subClassOf] Platelet Membrane Fluidity [subClassOf] Polyglucosan Body Myopathy [subClassOf] Polymicrogyria [subClassOf] Polyposis [subClassOf] Polyposis Syndrome, Hereditary Mixed [subClassOf] Polysubstance Abuse, Susceptibility To [subClassOf] Pontocerebellar Hypoplasia, Type 2F; PCH2F [subClassOf] Precocious Puberty [subClassOf] Pregnancy Loss, Recurrent, Susceptibility [subClassOf] Preimplantation Embryonic Lethality; PREMBL [subClassOf] Premature Aging Syndrome [subClassOf] Progeroid Syndrome [subClassOf] Progressive Familial Heart Block [subClassOf] Protein Z Deficiency [subClassOf] Proteolytic Capacity Of Plasma [subClassOf] Protocadherin 3 [subClassOf] Pulmonary Hypertension, Neonatal, Susceptibility To [subClassOf] Pulmonary Surfactant Metabolism Dysfunction [subClassOf] Pygmy [subClassOf] Radioulnar Synostosis With Amegakaryocytic Thrombocytopenia [subClassOf] Radioulnar Synostosis, Radial Ray Abnormalities, And Severe Malformations 1N The Male [subClassOf] Rare Abdominal Surgical Disease [subClassOf] Rare Cardiac Disease [subClassOf] Rare Circulatory System Disease [subClassOf] Rare Developmental Defect During Embryogenesis [subClassOf] Rare Gastroenterologic Disease [subClassOf] Rare Genetic Cardiac Disease [subClassOf] Rare Genetic Developmental Defect During Embryogenesis [subClassOf] Rare Genetic Gastroenterological Disease [subClassOf] Rare Genetic Gynecological And Obstetrical Diseases [subClassOf] Rare Genetic Hematologic Disease [subClassOf] Rare Genetic Neurological Disorder [subClassOf] Rare Genetic Odontologic Disease [subClassOf] Rare Genetic Renal Disease [subClassOf] Rare Genetic Systemic Or Rheumatologic Disease [subClassOf] Rare Genetic Urogenital Disease [subClassOf] Rare Gynecologic Or Obstetric Disease [subClassOf] Rare Intoxication [subClassOf] Rare Maxillo-Facial Surgical Disease [subClassOf] Rare Neoplastic Disease [subClassOf] Rare Odontologic Disease [subClassOf] Rare Otorhinolaryngologic Disease [subClassOf] Rare Renal Disease [subClassOf] Rare Surgical Thoracic Disease [subClassOf] Rare Systemic Or Rheumatologic Disease [subClassOf] Rare Urogenital Disease [subClassOf] Regeneration-Associated Serpin-1 [subClassOf] Renal Dysplasia, Cystic, Susceptibility To [subClassOf] Renal Hypodysplasia/Aplasia [subClassOf] Renal And Mullerian Duct Hypoplasia [subClassOf] Respiratory Underresponsiveness To Hypoxia And Hypercapnia [subClassOf] Reticulate Pigment Disorder [subClassOf] Retinal Dystrophy And Iris Coloboma With Or Without Congenital Cataract; [subClassOf] Retinitis Pigmentosa And Erythrocytic Microcytosis; RPEM [subClassOf] Retinopathy [subClassOf] Retinopathy, Pigmentary, And Mental Retardation [subClassOf] Rheumatoid Nodulosis [subClassOf] Rhiny [subClassOf] Ritscher-Schinzel Syndrome [subClassOf] Rudiger Syndrome [subClassOf] Salivary Substance, Clostridium Botulinum Type [subClassOf] Schindler Disease [subClassOf] Schistosoma Mansoni Infection, Susceptibility [subClassOf] Seizures, Cortical Blindness, Microcephaly Syndrome; SCBMS [subClassOf] Seizures, Scoliosis, And Macrocephaly Syndrome; SSMS [subClassOf] Senile Plaque Formation [subClassOf] Severe Cutaneous Adverse Reaction, Susceptibility To [subClassOf] Short Stature With Microcephaly And Distinctive Facies [subClassOf] Short Stature With Nonspecific Skeletal Abnormalities [subClassOf] Short Stature, Developmental Delay, And Congenital Heart Defects; [subClassOf] Short Stature, Microcephaly, And Endocrine Dysfunction [subClassOf] Short-Rib Thoracic Dysplasia [subClassOf] Short-Rib Thoracic Dysplasia 14 With Polydactyly [subClassOf] Singleton-Merten Syndrome [subClassOf] Sister Chromatid Exchange, Frequency Of [subClassOf] Sjogren-Larsson-Like Ichthyosis Without Cns Or Eye Involvement [subClassOf] Skin Creases, Congenital Symmetric Circumferential [subClassOf] Skint1-Like Pseudogene [subClassOf] Smith-Kingsmore Syndrome; SKS [subClassOf] Sodium-Potassium-Atpase Activity Of Red Cell [subClassOf] Somatomedin, Embryonic [subClassOf] Spastic Paraplegia And Psychomotor Retardation With Or Without Seizures; [subClassOf] Spastic Paraplegia, Optic Atrophy, Microcephaly, And 10Y Sex Reversal [subClassOf] Speech-Sound Disorder [subClassOf] Sperm Protamine P4 [subClassOf] Sperm-Specific Antigen 1 [subClassOf] Spherocytosis [subClassOf] Spinal Muscular Atrophy With Congenital Bone Fractures [subClassOf] Spinocerebellar Degeneration With Slow Eye Movements [subClassOf] Split-Foot Malformation With Mesoaxial Polydactyly; SFMMP [subClassOf] Split-Hand/Foot Malformation [subClassOf] Split-Hand/Foot Malformation With Long Bone Deficiency [subClassOf] Spondyloepimetaphyseal Dysplasia With Joint Laxity [subClassOf] Spondyloepimetaphyseal Dysplasia, Faden-Alkuraya Type; SEMDFA [subClassOf] Sternum, Premature Obliteration Of Sutures Of [subClassOf] Stomatin-Like Protein-2, Hyperphosphorylation Of [subClassOf] Streptococcus, Group A, Severity Of Infection By [subClassOf] Striae Distensae, Familial [subClassOf] Striatal Degeneration, Autosomal Dominant [subClassOf] Striatonigral Degeneration, Childhood-Onset; SNDC [subClassOf] Sugarman Brachydactyly [subClassOf] Surface Antigen, Glycoprotein 75 [subClassOf] Surface Polypeptides, Anonymous [subClassOf] Symphalangism [subClassOf] T-Box 24 [subClassOf] T-Cell Subgroups, Non-Hla-Linked [subClassOf] T-Complex Locus Tcp10B [subClassOf] T-Substance Anomaly [subClassOf] Takenouchi-Kosaki Syndrome; TKS [subClassOf] Taqi Polymorphism [subClassOf] Tardive Dyskinesia [subClassOf] Tarsal Coalition [subClassOf] Tear Protein, Anodal [subClassOf] Teeth Present At Birth [subClassOf] Teeth, Supernumerary [subClassOf] Temperature-Sensitive Lethal Mutation [subClassOf] Tenorio Syndrome [subClassOf] Testes, Rudimentary [subClassOf] Thalidomide Susceptibility [subClassOf] Theophylline Biotransformation [subClassOf] Thiamine-Responsive Dysfunction Syndrome [subClassOf] Thiopurines, Poor Metabolism Of [subClassOf] Threoninemia [subClassOf] Thumb, Distal Hyperextensibility Of [subClassOf] Thumbs, Congenital Clasped [subClassOf] Thyroid Cancer, Nonmedullary [subClassOf] Thyroid Dyshormonogenesis [subClassOf] Tibia, Hypoplasia Or Aplasia Of, With Polydactyly [subClassOf] Tibial Torsion, Bilateral Medial [subClassOf] Tinea Imbricata, Susceptibility To [subClassOf] Tl Antigen [subClassOf] Tn Polyagglutination Syndrome [subClassOf] Toe, Fifth, Number Of Phalanges 1N [subClassOf] Toe, Misshapen [subClassOf] Toe, Rotated Fifth [subClassOf] Toes, Relative Length Of First And Second [subClassOf] Toes, Space Between First And Second [subClassOf] Tongue, Pigmented Fungiform Papillae Of [subClassOf] Transposition Of The Great Arteries [subClassOf] Trichohepatoenteric Syndrome [subClassOf] Trichomegaly [subClassOf] Trichorhinophalangeal Syndrome [subClassOf] Trigger Thumb [subClassOf] Triglyceride Storage Disease [subClassOf] Trigonocephaly [subClassOf] Tristichiasis [subClassOf] Tuberculin Skin Test Reactivity, Absence Of [subClassOf] Tubulin, Beta [subClassOf] Ubiquitin-Activating Enzyme, Y-Linked [subClassOf] Umbilicus, Familial Flat [subClassOf] Unique Green Phenomenon [subClassOf] Urate-Binding Globulin, Decrease 1N [subClassOf] Ureter, Bifid Or Double [subClassOf] Urinary Bladder, Atony Of [subClassOf] Urinary Tract Infections, Recurrent, Susceptibility To [subClassOf] Urolithiasis, Uric Acid, Autosomal Dominant [subClassOf] Uterine Anomalies [subClassOf] Uvula, Bifid [subClassOf] Vascular Helix Of Umbilical Cord [subClassOf] Veins, Pattern Of, On Anterior Thorax [subClassOf] Ventricular Fibrillation [subClassOf] Ventricular Tachycardia, Catecholaminergic Polymorphic [subClassOf] Vertigo [subClassOf] Virus Rd114 Rna Complementarity [subClassOf] Vitamin K-Dependent Clotting Factors, Combined Deficiency Of [subClassOf] Webb-Dattani Syndrome [subClassOf] Widow'S Peak [subClassOf] Wilms Tumor [subClassOf] Woronets Trait [subClassOf] X-Linked B Cell Surface Antigen, Mouse, Homolog-Like 1 [subClassOf] Xh Antigen [subClassOf] You-Hoover-Fong Syndrome; YHFS [subClassOf] Yuan-Harel-Lupski Syndrome; YUHAL [subClassOf] Zimmermann-Laband Syndrome [subClassOf] Disease By Infectious Agent [subClassOf] Disease Of Anatomical Entity [subClassOf] Disease Of Cellular Proliferation [subClassOf] Disease Of Mental Health [subClassOf] Disease Of Metabolism [subClassOf] Genetic Disease [subClassOf] Physical Disorder

cmungall commented 7 years ago

With IDs:

It's not a browser issue, this is what it looks like. obviously terrible for top-down browsing

nicolevasilevsky commented 6 years ago

The hierarchy has changed since this was opened a year ago- closing this ticket.