disease ontology - Robuta Search

https://disease-ontology.org/?id=DOID:0061131 Disease Ontology - Institute for Genome Sciences @ University of Maryland university of maryland disease ontology institute genome sciences https://disease-ontology.org/?id=DOID:0070749 Disease Ontology - Institute for Genome Sciences @ University of Maryland university of maryland disease ontology institute genome sciences https://www.pombase.org/term/MONDO:0024189 PomBase - Disease association ontology term - MONDO:0024189 - neurologic, endocrine, and pancreatic... PomBase - Disease association ontology term - MONDO:0024189 - neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset - The... pombase disease association ontology term https://disease-ontology.org/?id=DOID:0070709 Disease Ontology - Institute for Genome Sciences @ University of Maryland university of maryland disease ontology institute genome sciences https://www.pombase.org/term/MONDO:0018630 PomBase - Disease association ontology term - MONDO:0018630 - hereditary nonpolyposis colon cancer... PomBase - Disease association ontology term - MONDO:0018630 - hereditary nonpolyposis colon cancer - The Schizosaccharomyces pombe genome database colon cancer pombase disease association ontology https://www.pombase.org/term/MONDO:0032712 PomBase - Disease association ontology term - MONDO:0032712 - combined oxidative phosphorylation... PomBase - Disease association ontology term - MONDO:0032712 - combined oxidative phosphorylation deficiency 38 - The Schizosaccharomyces pombe genome database oxidative phosphorylation pombase disease association ontology https://www.pombase.org/term/MONDO:0010043 PomBase - Disease association ontology term - MONDO:0010043 - hereditary spastic paraplegia 17 -... PomBase - Disease association ontology term - MONDO:0010043 - hereditary spastic paraplegia 17 - The Schizosaccharomyces pombe genome database hereditary spastic paraplegia pombase disease association ontology https://www.pombase.org/term/MONDO:0005500 PomBase - Disease association ontology term - MONDO:0005500 - congenital disorder of glycosylation... PomBase - Disease association ontology term - MONDO:0005500 - congenital disorder of glycosylation type I - The Schizosaccharomyces pombe genome database congenital disorder pombase disease association ontology https://www.semanticjuice.com/diabetes/disease-ontology.org disease-ontology.org - Diabetes disease-ontology.org - Diabetes . niche, top domains and resources disease ontology diabetes https://www.disease-ontology.org/?id=DOID:0110594 Disease Ontology - Institute for Genome Sciences @ University of Maryland university of maryland disease ontology institute genome sciences https://www.disease-ontology.org/?id=DOID:0080518 Disease Ontology - Institute for Genome Sciences @ University of Maryland university of maryland disease ontology institute genome sciences https://disease-ontology.org/?id=DOID:0061273 Disease Ontology - Institute for Genome Sciences @ University of Maryland university of maryland disease ontology institute genome sciences https://www.informatics.jax.org/disease/DOID:0080448 developmental and epileptic encephalopathy 48 Disease Ontology Browser - DOID:0080448 Mutations in human and/or mouse homologs are associated with this disease. Synonyms: DEE48; early infantile epileptic encephalopathy 48 disease ontology developmental epileptic encephalopathy browser https://www.pombase.org/term/MONDO:0000732 PomBase - Disease association ontology term - MONDO:0000732 - combined oxidative phosphorylation... PomBase - Disease association ontology term - MONDO:0000732 - combined oxidative phosphorylation deficiency - The Schizosaccharomyces pombe genome database oxidative phosphorylation pombase disease association ontology https://www.pombase.org/term/MONDO:0019053 PomBase - Disease association ontology term - MONDO:0019053 - peroxisomal disease - The... PomBase - Disease association ontology term - MONDO:0019053 - peroxisomal disease - The Schizosaccharomyces pombe genome database pombase disease association ontology term https://www.pombase.org/term/MONDO:0024517 PomBase - Disease association ontology term - MONDO:0024517 - SMARCB1-related schwannomatosis - The... PomBase - Disease association ontology term - MONDO:0024517 - SMARCB1-related schwannomatosis - The Schizosaccharomyces pombe genome database pombase disease association ontology term https://www.pombase.org/term/MONDO:0016033 PomBase - Disease association ontology term - MONDO:0016033 - Cornelia de Lange syndrome - The... PomBase - Disease association ontology term - MONDO:0016033 - Cornelia de Lange syndrome - The Schizosaccharomyces pombe genome database cornelia de lange pombase disease association ontology https://www.pombase.org/term/MONDO:0014394 PomBase - Disease association ontology term - MONDO:0014394 - Diamond-Blackfan anemia 13 - The... PomBase - Disease association ontology term - MONDO:0014394 - Diamond-Blackfan anemia 13 - The Schizosaccharomyces pombe genome database diamond blackfan anemia pombase disease association ontology https://publica.fraunhofer.de/entities/publication/a1fa5fa1-6f81-4892-87ed-f7e4345a7731 Design of the formalized and integrated Alzheimer's Disease Ontology and its application in... As one of the leading causes for dementia in the population, it is imperative that we discern exactly why Alzheimer’s disease (AD) has a strong molecular... of the disease ontology design formalized integrated https://www.pombase.org/term/MONDO:0014985 PomBase - Disease association ontology term - MONDO:0014985 - Fanconi anemia complementation group... PomBase - Disease association ontology term - MONDO:0014985 - Fanconi anemia complementation group V - The Schizosaccharomyces pombe genome database fanconi anemia pombase disease association ontology https://www.informatics.jax.org/disease/DOID:0111973 immunodeficiency 17 Disease Ontology Browser - DOID:0111973 Mutations in human and/or mouse homologs are associated with this disease. Synonyms: CD3-gamma deficiency; IMD17; immunodeficiency 17, CD3 gamma deficient;... disease ontology immunodeficiency browser doid https://www.pombase.org/term/MONDO:0032911 PomBase - Disease association ontology term - MONDO:0032911 - hearing loss, autosomal dominant 75 -... PomBase - Disease association ontology term - MONDO:0032911 - hearing loss, autosomal dominant 75 - The Schizosaccharomyces pombe genome database hearing loss autosomal dominant pombase disease association https://www.informatics.jax.org/disease/DOID:0080791 Treacher Collins syndrome 3 Disease Ontology Browser - DOID:0080791 Mutations in human and/or mouse homologs are associated with this disease. treacher collins syndrome disease ontology browser doid https://www.informatics.jax.org/disease/DOID:0110421 late-adult onset retinitis pigmentosa Disease Ontology Browser - DOID:0110421 There are currently no human or mouse genes associated with this disease in the MGI database. Synonyms: senile retinitis pigmentosa adult onset retinitis pigmentosa disease ontology late browser https://www.disease-ontology.org/?id=DOID:0110355 Disease Ontology - Institute for Genome Sciences @ University of Maryland university of maryland disease ontology institute genome sciences https://disease-ontology.org/?id=DOID:0080110 Disease Ontology - Institute for Genome Sciences @ University of Maryland university of maryland disease ontology institute genome sciences https://www.pombase.org/term/MONDO:0015753 PomBase - Disease association ontology term - MONDO:0015753 - cap myopathy - The... PomBase - Disease association ontology term - MONDO:0015753 - cap myopathy - The Schizosaccharomyces pombe genome database pombase disease association ontology term https://www.disease-ontology.org/?id=DOID:0060733 Disease Ontology - Institute for Genome Sciences @ University of Maryland university of maryland disease ontology institute genome sciences