FRINK Linked Data Fragments server

Matches in Ubergraph for { ?s <http://www.w3.org/2000/01/rdf-schema#seeAlso> ?o ?g. }

• MONDO_0008555 seeAlso "https://rarediseases.info.nih.gov/diseases/5191/thrombocytopenia-2" @default.
• MONDO_0008556 seeAlso "https://rarediseases.info.nih.gov/diseases/9862/cyclic-thrombocytopenia" @default.
• MONDO_0008557 seeAlso "https://rarediseases.info.nih.gov/diseases/4224/paris-trousseau-thrombocytopenia" @default.
• MONDO_0008565 seeAlso "https://rarediseases.info.nih.gov/diseases/5204/familial-thyroglossal-duct-cyst" @default.
• MONDO_0008568 seeAlso "https://rarediseases.info.nih.gov/diseases/8499/thyroid-hormone-plasma-membrane-transport-defect" @default.
• MONDO_0008583 seeAlso "https://rarediseases.info.nih.gov/diseases/4908/congenital-torticollis" @default.
• MONDO_0008585 seeAlso "https://rarediseases.info.nih.gov/diseases/8528/hellp-syndrome" @default.
• MONDO_0008588 seeAlso "https://rarediseases.info.nih.gov/diseases/9501/hereditary-geniospasm" @default.
• MONDO_0008592 seeAlso "https://rarediseases.info.nih.gov/diseases/7799/tricho-dento-osseous-syndrome" @default.
• MONDO_0008599 seeAlso "https://rarediseases.info.nih.gov/diseases/7805/trigeminal-neuralgia" @default.
• MONDO_0008600 seeAlso "https://rarediseases.info.nih.gov/diseases/8484/trigger-thumb" @default.
• MONDO_0008606 seeAlso "https://rarediseases.info.nih.gov/diseases/242/say-field-coldwell-syndrome" @default.
• MONDO_0008611 seeAlso "https://rarediseases.info.nih.gov/diseases/2750/trochlea-of-the-humerus-aplasia-of" @default.
• MONDO_0008619 seeAlso "https://rarediseases.info.nih.gov/diseases/4740/ulna-metaphyseal-dysplasia-syndrome" @default.
• MONDO_0008621 seeAlso "https://rarediseases.info.nih.gov/diseases/5404/uncombable-hair-syndrome" @default.
• MONDO_0008624 seeAlso "https://rarediseases.info.nih.gov/diseases/5421/upington-disease" @default.
• MONDO_0008632 seeAlso "https://rarediseases.info.nih.gov/diseases/10901/aquagenic-urticaria" @default.
• MONDO_0008640 seeAlso "https://rarediseases.info.nih.gov/diseases/6941/lymphocytic-vasculitis" @default.
• MONDO_0008641 seeAlso "https://rarediseases.info.nih.gov/diseases/10535/hereditary-vascular-retinopathy" @default.
• MONDO_0008641 seeAlso "https://rarediseases.info.nih.gov/diseases/1217/retinal-vasculopathy-with-cerebral-leukodystrophy" @default.
• MONDO_0008641 seeAlso "https://rarediseases.info.nih.gov/diseases/2558/grand-kaine-fulling-syndrome" @default.
• MONDO_0008650 seeAlso "https://rarediseases.info.nih.gov/diseases/2276/faulk-epstein-jones-syndrome" @default.
• MONDO_0008652 seeAlso "https://rarediseases.info.nih.gov/diseases/5488/congenital-vertical-talus" @default.
• MONDO_0008655 seeAlso "https://rarediseases.info.nih.gov/diseases/5489/vestibulocochlear-dysfunction-progressive" @default.
• MONDO_0008659 seeAlso "https://rarediseases.info.nih.gov/diseases/5239/transcobalamin-1-deficiency" @default.
• MONDO_0008663 seeAlso "https://rarediseases.info.nih.gov/diseases/9706/snowflake-vitreoretinal-degeneration" @default.
• MONDO_0008667 seeAlso "https://rarediseases.info.nih.gov/diseases/7855/von-hippel-lindau-disease" @default.
• MONDO_0008670 seeAlso "https://rarediseases.info.nih.gov/diseases/5519/waardenburg-syndrome-type-1" @default.
• MONDO_0008671 seeAlso "https://rarediseases.info.nih.gov/diseases/5521/waardenburg-syndrome-type-2a" @default.
• MONDO_0008672 seeAlso "https://rarediseases.info.nih.gov/diseases/5540/watson-syndrome" @default.
• MONDO_0008680 seeAlso "https://rarediseases.info.nih.gov/diseases/8559/familial-wilms-tumor-2" @default.
• MONDO_0008681 seeAlso "https://rarediseases.info.nih.gov/diseases/5528/wagr-syndrome" @default.
• MONDO_0008684 seeAlso "https://rarediseases.info.nih.gov/diseases/7896/wolf-hirschhorn-syndrome" @default.
• MONDO_0008688 seeAlso "https://rarediseases.info.nih.gov/diseases/39/wt-limb-blood-syndrome" @default.
• MONDO_0008689 seeAlso "https://rarediseases.info.nih.gov/diseases/10676/dehydrated-hereditary-stomatocytosis-pseudohyperkalemia-and-perinatal-edema" @default.
• MONDO_0008694 seeAlso "https://rarediseases.info.nih.gov/diseases/415/pseudoprogeria-syndrome" @default.
• MONDO_0008699 seeAlso "https://rarediseases.info.nih.gov/diseases/456/achalasia-microcephaly-syndrome" @default.
• MONDO_0008704 seeAlso "https://rarediseases.info.nih.gov/diseases/2988/achondroplasia-and-severe-combined-immunodeficiency" @default.
• MONDO_0008706 seeAlso "https://rarediseases.info.nih.gov/diseases/469/ackerman-syndrome" @default.
• MONDO_0008711 seeAlso "https://rarediseases.info.nih.gov/diseases/2549/goodman-syndrome" @default.
• MONDO_0008713 seeAlso "https://rarediseases.info.nih.gov/diseases/5723/acrodermatitis-enteropathica" @default.
• MONDO_0008713 seeAlso "https://rarediseases.info.nih.gov/diseases/6343/enteropathica" @default.
• MONDO_0008714 seeAlso "https://rarediseases.info.nih.gov/diseases/496/acrofacial-dysostosis-rodriguez-type" @default.
• MONDO_0008722 seeAlso "https://rarediseases.info.nih.gov/diseases/4822/short-chain-acyl-coa-dehydrogenase-deficiency" @default.
• MONDO_0008730 seeAlso "https://rarediseases.info.nih.gov/diseases/1469/17-alpha-hydroxylase-deficiency" @default.
• MONDO_0008733 seeAlso "https://rarediseases.info.nih.gov/diseases/2498/familial-glucocorticoid-deficiency" @default.
• MONDO_0008742 seeAlso "https://rarediseases.info.nih.gov/diseases/9558/severe-congenital-neutropenia-autosomal-dominant" @default.
• MONDO_0008746 seeAlso "https://rarediseases.info.nih.gov/diseases/4038/oculocutaneous-albinism-type-2" @default.
• MONDO_0008749 seeAlso "https://rarediseases.info.nih.gov/diseases/10682/pseudohypoparathyroidism-type-2" @default.
• MONDO_0008750 seeAlso "https://rarediseases.info.nih.gov/diseases/3604/microcephaly-albinism-digital-anomalies-syndrome" @default.
• MONDO_0008751 seeAlso "https://rarediseases.info.nih.gov/diseases/5660/18-hydroxylase-deficiency" @default.
• MONDO_0008752 seeAlso "https://rarediseases.info.nih.gov/diseases/5774/alexander-disease" @default.
• MONDO_0008753 seeAlso "https://rarediseases.info.nih.gov/diseases/5775/alkaptonuria" @default.
• MONDO_0008754 seeAlso "https://rarediseases.info.nih.gov/diseases/605/alopecia-contractures-dwarfism-intellectual-disability-syndrome" @default.
• MONDO_0008762 seeAlso "https://rarediseases.info.nih.gov/diseases/625/autosomal-recessive-alport-syndrome" @default.
• MONDO_0008765 seeAlso "https://rarediseases.info.nih.gov/diseases/636/leber-congenital-amaurosis-2" @default.
• MONDO_0008766 seeAlso "https://rarediseases.info.nih.gov/diseases/637/amaurosis-congenita-cone-rod-type-with-congenital-hypertrichosis" @default.
• MONDO_0008772 seeAlso "https://rarediseases.info.nih.gov/diseases/9495/amelogenesis-imperfecta-pigmented-hypomaturation-type" @default.
• MONDO_0008773 seeAlso "https://rarediseases.info.nih.gov/diseases/763/amino-aciduria-with-mental-deficiency-dwarfism-muscular-dystrophy-osteoporosis-and-acidosis" @default.
• MONDO_0008776 seeAlso "https://rarediseases.info.nih.gov/diseases/657/amyloidosis-of-gingiva-and-conjunctiva-with-intellectual-disability" @default.
• MONDO_0008777 seeAlso "https://rarediseases.info.nih.gov/diseases/9647/amyloidosis-corneal" @default.
• MONDO_0008780 seeAlso "https://rarediseases.info.nih.gov/diseases/9470/amyotrophic-lateral-sclerosis-type-2" @default.
• MONDO_0008793 seeAlso "https://rarediseases.info.nih.gov/diseases/8587/angiomatosis-diffuse-corticomeningeal-of-divry-and-van-bogaert" @default.
• MONDO_0008797 seeAlso "https://rarediseases.info.nih.gov/diseases/5818/anodontia" @default.
• MONDO_0008803 seeAlso "https://rarediseases.info.nih.gov/diseases/5826/antley-bixler-syndrome" @default.
• MONDO_0008809 seeAlso "https://rarediseases.info.nih.gov/diseases/2589/hamanishi-ueba-tsuji-syndrome" @default.
• MONDO_0008811 seeAlso "https://rarediseases.info.nih.gov/diseases/424/xk-aprosencephaly" @default.
• MONDO_0008813 seeAlso "https://rarediseases.info.nih.gov/diseases/17/arachnoid-cysts" @default.
• MONDO_0008815 seeAlso "https://rarediseases.info.nih.gov/diseases/5843/argininosuccinic-aciduria" @default.
• MONDO_0008824 seeAlso "https://rarediseases.info.nih.gov/diseases/9634/fetal-akinesia-deformation-sequence" @default.
• MONDO_0008828 seeAlso "https://rarediseases.info.nih.gov/diseases/306/camptodactyly-arthropathy-coxa-vara-pericarditis-syndrome" @default.
• MONDO_0008829 seeAlso "https://rarediseases.info.nih.gov/diseases/1359/chylous-ascites" @default.
• MONDO_0008840 seeAlso "https://rarediseases.info.nih.gov/diseases/5862/ataxia-telangiectasia" @default.
• MONDO_0008846 seeAlso "https://rarediseases.info.nih.gov/diseases/9595/atransferrinemia" @default.
• MONDO_0008849 seeAlso "https://rarediseases.info.nih.gov/diseases/9744/atrophoderma-vermiculata" @default.
• MONDO_0008853 seeAlso "https://rarediseases.info.nih.gov/diseases/819/barber-say-syndrome" @default.
• MONDO_0008855 seeAlso "https://rarediseases.info.nih.gov/diseases/824/bare-lymphocyte-syndrome-2" @default.
• MONDO_0008857 seeAlso "https://rarediseases.info.nih.gov/diseases/846/beemer-ertbruggen-syndrome" @default.
• MONDO_0008858 seeAlso "https://rarediseases.info.nih.gov/diseases/849/behr-syndrome" @default.
• MONDO_0008859 seeAlso "https://rarediseases.info.nih.gov/diseases/8552/berry-aneurysm-cirrhosis-pulmonary-emphysema-and-cerebral-calcification" @default.
• MONDO_0008861 seeAlso "https://rarediseases.info.nih.gov/diseases/5665/3-methylcrotonyl-coa-carboxylase-1-deficiency" @default.
• MONDO_0008863 seeAlso "https://rarediseases.info.nih.gov/diseases/7653/sitosterolemia" @default.
• MONDO_0008864 seeAlso "https://rarediseases.info.nih.gov/diseases/882/biemond-syndrome-2" @default.
• MONDO_0008865 seeAlso "https://rarediseases.info.nih.gov/diseases/10050/bietti-crystalline-corneoretinal-dystrophy" @default.
• MONDO_0008867 seeAlso "https://rarediseases.info.nih.gov/diseases/12010/biliary-atresia" @default.
• MONDO_0008872 seeAlso "https://rarediseases.info.nih.gov/diseases/9844/microcephalic-osteodysplastic-primordial-dwarfism-type-2" @default.
• MONDO_0008874 seeAlso "https://rarediseases.info.nih.gov/diseases/812/bangstad-syndrome" @default.
• MONDO_0008876 seeAlso "https://rarediseases.info.nih.gov/diseases/915/bloom-syndrome" @default.
• MONDO_0008877 seeAlso "https://rarediseases.info.nih.gov/diseases/5939/blue-diaper-syndrome" @default.
• MONDO_0008878 seeAlso "https://rarediseases.info.nih.gov/diseases/922/bone-dysplasia-lethal-holmgren-type" @default.
• MONDO_0008879 seeAlso "https://rarediseases.info.nih.gov/diseases/5950/bowen-conradi-syndrome" @default.
• MONDO_0008881 seeAlso "https://rarediseases.info.nih.gov/diseases/10149/kyphomelic-dysplasia" @default.
• MONDO_0008882 seeAlso "https://rarediseases.info.nih.gov/diseases/953/bowing-of-long-bones-congenital" @default.
• MONDO_0008884 seeAlso "https://rarediseases.info.nih.gov/diseases/992/brachymetapody-anodontia-hypotrichosis-albinoidism" @default.
• MONDO_0008886 seeAlso "https://rarediseases.info.nih.gov/diseases/313/sabinas-brittle-hair-syndrome" @default.
• MONDO_0008890 seeAlso "https://rarediseases.info.nih.gov/diseases/10928/progressive-bulbar-palsy" @default.
• MONDO_0008891 seeAlso "https://rarediseases.info.nih.gov/diseases/9993/riboflavin-transporter-deficiency" @default.
• MONDO_0008893 seeAlso "https://rarediseases.info.nih.gov/diseases/5978/c-syndrome" @default.
• MONDO_0008896 seeAlso "https://rarediseases.info.nih.gov/diseases/1061/campomelia-cumming-type" @default.
• MONDO_0008898 seeAlso "https://rarediseases.info.nih.gov/diseases/1067/camptodactyly-syndrome-guadalajara-type-1" @default.

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