Robuta

https://www.informatics.jax.org/disease/601634 neural tube defect Disease Ontology Browser - DOID:0080074 Mutations in human and/or mouse homologs are associated with this disease. ontology browserneuraltubedefectdisease https://www.tambang.co.id/dukung-kesiapan-tenaga-kerja-anak-usaha-doid-bangun-falisitas-pelatihan-dan-tes/ Dukung Kesiapan Tenaga Kerja, Anak Usaha DOID Bangun Falisitas Pelatihan Dan Tes Apr 17, 2026 - Jakarta,TAMBANG,- PT BISA Ruang Nuswantara (BIRU) meresmikan Pusat Pelatihan (Training Center) terintegrasi di Depok, Jawa Barat dan Pusat Tes (Test Center) di... tenaga kerjaanak usaha https://www.informatics.jax.org/disease/DOID:0061076 immunodeficiency 107 Disease Ontology Browser - DOID:0061076 Mutations in human and/or mouse homologs are associated with this disease. Synonyms: immunodeficiency 107 with susceptibility to invasive Staphylococcus aureus... ontology browserimmunodeficiencydiseasedoid https://blogs.imperial.ac.uk/doid-staff/tag/coronavirus/ coronavirus Archives - DoID Staff Blog coronavirusarchivesdoidstaffblog https://www.mousemine.org/mousemine/report.do;jsessionid=D6200FF5400E66A28C458FE76BFCA078?id=95049299&trail=%7C95049299 MouseMine: DOTerm Parkinson's disease 21 DOID:0111251 Disease Ontology parkinsondiseasedoidontology https://www.informatics.jax.org/disease/DOID:0081356 spinal muscular atrophy, Jokela type Disease Ontology Browser - DOID:0081356 Mutations in human and/or mouse homologs are associated with this disease. spinal muscular atrophyontology browsertypediseasedoid https://www.informatics.jax.org/disease/DOID:0070438 retinal macular dystrophy Disease Ontology Browser - DOID:0070438 Mutations in human and/or mouse homologs are associated with this disease. Synonyms: MCDR ontology browserretinaldiseasedoid https://www.informatics.jax.org/disease/DOID:0111438 optic atrophy 5 Disease Ontology Browser - DOID:0111438 Mutations in human and/or mouse homologs are associated with this disease. Synonyms: OPA5 optic atrophyontology browserdiseasedoid https://www.informatics.jax.org/disease/DOID:0110427 dilated cardiomyopathy 1V Disease Ontology Browser - DOID:0110427 Mutations in human and/or mouse homologs are associated with this disease. Synonyms: CMD1V dilated cardiomyopathyontology browserdiseasedoid https://www.informatics.jax.org/disease/DOID:1470 major depressive disorder Disease Ontology Browser - DOID:1470 Mutations in human and/or mouse homologs are associated with this disease. Synonyms: clinical depression; major depression; recurrent major depression; single... major depressive disorderontology browserdiseasedoid https://www.informatics.jax.org/disease/DOID:0070211 hereditary lymphedema IB Disease Ontology Browser - DOID:0070211 There are currently no human or mouse genes associated with this disease in the MGI database. Synonyms: LMPH1B ontology browserhereditarylymphedemaibdisease https://www.informatics.jax.org/disease/DOID:0070471 early-onset epilepsy 2 Disease Ontology Browser - DOID:0070471 Mutations in human and/or mouse homologs are associated with this disease. Synonyms: early-onset epilepsy-2 with or without developmental delay; EPEO2 early onsetontology browserepilepsydiseasedoid https://nadh.in/blog/decentralised-open-indexes/ Decentralised Open Indexes for Discovery (DOID) - nadh.in A conceptual and technical framework for resource discovery on the WWW using decentralised, open, machine-readable indexes as the building block. decentralisedopenindexesdiscoverydoid https://www.informatics.jax.org/disease/DOID:14693 Clouston syndrome Disease Ontology Browser - DOID:14693 Mutations in human and/or mouse homologs are associated with this disease. Synonyms: Clouston's hidrotic ectodermal dysplasia; Clouston's syndrome; ectodermal... ontology browsersyndromediseasedoid https://www.informatics.jax.org/disease/DOID:0060585 Noonan syndrome 7 Disease Ontology Browser - DOID:0060585 Mutations in human and/or mouse homologs are associated with this disease. Synonyms: NS7 noonan syndromeontology browserdiseasedoid https://galerisaham.com/analisa-fundamental-saham-doid/ Analisa Fundamental Saham DOID Nov 28, 2016 - Berikut adalah ulasan fundamental DOID yang diolah oleh tim GS PRO ketika berada di level 450-an dan masih relevan hingga saat ini. DOID mengalami peningkatan... analisafundamentalsahamdoid https://www.informatics.jax.org/disease/DOID:0050855 renal fibrosis Disease Ontology Browser - DOID:0050855 Mutations in human and/or mouse homologs are associated with this disease. ontology browserrenalfibrosisdiseasedoid https://www.mousemine.org/mousemine/report.do;jsessionid=D6200FF5400E66A28C458FE76BFCA078?id=77291629&trail=%7C77291629 MouseMine: DOTerm Parkinson's disease 8 DOID:0060371 Disease Ontology parkinsondiseasedoidontology https://www.informatics.jax.org/disease/DOID:0070636 mirror movements 1 Disease Ontology Browser - DOID:0070636 Mutations in human and/or mouse homologs are associated with this disease. ontology browsermirrormovementsdiseasedoid https://www.informatics.jax.org/disease/DOID:11984 hypertrophic cardiomyopathy Disease Ontology Browser - DOID:11984 Mutations in human and/or mouse homologs are associated with this disease. Synonyms: hypertrophic obstructive cardiomyopathy hypertrophic cardiomyopathyontology browserdiseasedoid https://www.informatics.jax.org/disease/DOID:0050606 acrokeratosis verruciformis Disease Ontology Browser - DOID:0050606 Mutations in human and/or mouse homologs are associated with this disease. Synonyms: Acrokeratosis verruciformis of Hopf; Hopf disease ontology browserdiseasedoid https://www.informatics.jax.org/disease/DOID:0070578 spermatogenic failure 79 Disease Ontology Browser - DOID:0070578 Mutations in human and/or mouse homologs are associated with this disease. Synonyms: SPGF79 ontology browserfailurediseasedoid https://www.informatics.jax.org/disease/DOID:0111251 Parkinson's disease 21 Disease Ontology Browser - DOID:0111251 There are currently no human or mouse genes associated with this disease in the MGI database. Synonyms: PARK21; Parkinson disease 21 ontology browserparkinsondiseasedoid