FRINK Linked Data Fragments server

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

• MONDO_0012477 seeAlso "https://rarediseases.info.nih.gov/diseases/10400/retinitis-pigmentosa-33" @default.
• MONDO_0012481 seeAlso "https://rarediseases.info.nih.gov/diseases/3588/mevalonic-aciduria" @default.
• MONDO_0012501 seeAlso "https://rarediseases.info.nih.gov/diseases/8273/mutagen-sensitivity" @default.
• MONDO_0012502 seeAlso "https://rarediseases.info.nih.gov/diseases/10878/normophosphatemic-familial-tumoral-calcinosis" @default.
• MONDO_0012507 seeAlso "https://rarediseases.info.nih.gov/diseases/10650/retinal-cone-dystrophy-4" @default.
• MONDO_0012513 seeAlso "https://rarediseases.info.nih.gov/diseases/10661/maturity-onset-diabetes-of-the-young-type-7" @default.
• MONDO_0012519 seeAlso "https://rarediseases.info.nih.gov/diseases/10754/chromosome-16p133-deletion-syndrome" @default.
• MONDO_0012521 seeAlso "https://rarediseases.info.nih.gov/diseases/6649/herpes-simplex-encephalitis" @default.
• MONDO_0012523 seeAlso "https://rarediseases.info.nih.gov/diseases/10403/retinitis-pigmentosa-36" @default.
• MONDO_0012525 seeAlso "https://rarediseases.info.nih.gov/diseases/10489/leber-congenital-amaurosis-12" @default.
• MONDO_0012528 seeAlso "https://rarediseases.info.nih.gov/diseases/10772/kallmann-syndrome-4" @default.
• MONDO_0012529 seeAlso "https://rarediseases.info.nih.gov/diseases/10241/diamond-blackfan-anemia-3" @default.
• MONDO_0012532 seeAlso "https://rarediseases.info.nih.gov/diseases/10615/hereditary-hemorrhagic-telangiectasia-type-4" @default.
• MONDO_0012535 seeAlso "https://rarediseases.info.nih.gov/diseases/10055/holoprosencephaly-recurrent-infections-and-monocytosis" @default.
• MONDO_0012547 seeAlso "https://rarediseases.info.nih.gov/diseases/10699/noonan-syndrome-4" @default.
• MONDO_0012564 seeAlso "https://rarediseases.info.nih.gov/diseases/10456/polyosteolysishyperostosis-syndrome" @default.
• MONDO_0012572 seeAlso "https://rarediseases.info.nih.gov/diseases/9695/sakoda-complex" @default.
• MONDO_0012579 seeAlso "https://rarediseases.info.nih.gov/diseases/7499/autoimmune-pulmonary-alveolar-proteinosis" @default.
• MONDO_0012588 seeAlso "https://rarediseases.info.nih.gov/diseases/1220/neuronal-ceroid-lipofuscinosis-7" @default.
• MONDO_0012589 seeAlso "https://rarediseases.info.nih.gov/diseases/4372/pitt-hopkins-syndrome" @default.
• MONDO_0012590 seeAlso "https://rarediseases.info.nih.gov/diseases/10628/xfe-progeroid-syndrome" @default.
• MONDO_0012593 seeAlso "https://rarediseases.info.nih.gov/diseases/12163/brain-lung-thyroid-syndrome" @default.
• MONDO_0012621 seeAlso "https://rarediseases.info.nih.gov/diseases/11911/deafness-infertility-syndrome" @default.
• MONDO_0012638 seeAlso "https://rarediseases.info.nih.gov/diseases/9292/microphthalmia-syndromic-10" @default.
• MONDO_0012640 seeAlso "https://rarediseases.info.nih.gov/diseases/12443/charcot-marie-tooth-disease-type-4j" @default.
• MONDO_0012648 seeAlso "https://rarediseases.info.nih.gov/diseases/10223/isobutyryl-coa-dehydrogenase-deficiency" @default.
• MONDO_0012656 seeAlso "https://rarediseases.info.nih.gov/diseases/12644/lethal-congenital-contracture-syndrome-3" @default.
• MONDO_0012669 seeAlso "https://rarediseases.info.nih.gov/diseases/10714/legius-syndrome" @default.
• MONDO_0012675 seeAlso "https://rarediseases.info.nih.gov/diseases/13101/corticosteroid-binding-globulin-deficiency" @default.
• MONDO_0012676 seeAlso "https://rarediseases.info.nih.gov/diseases/5993/osteopetrosis-autosomal-recessive-4" @default.
• MONDO_0012679 seeAlso "https://rarediseases.info.nih.gov/diseases/4156/osteopetrosis-autosomal-recessive-6" @default.
• MONDO_0012683 seeAlso "https://rarediseases.info.nih.gov/diseases/10710/pontocerebellar-hypoplasia-type-6" @default.
• MONDO_0012690 seeAlso "https://rarediseases.info.nih.gov/diseases/10700/noonan-syndrome-5" @default.
• MONDO_0012713 seeAlso "https://rarediseases.info.nih.gov/diseases/4992/spondylometaphyseal-dysplasia-east-african-type" @default.
• MONDO_0012719 seeAlso "https://rarediseases.info.nih.gov/diseases/12505/encephalopathy-due-to-prosaposin-deficiency" @default.
• MONDO_0012720 seeAlso "https://rarediseases.info.nih.gov/diseases/10289/krabbe-disease-atypical-due-to-saposin-a-deficiency" @default.
• MONDO_0012721 seeAlso "https://rarediseases.info.nih.gov/diseases/2167/epilepsy-progressive-myoclonic-type-3" @default.
• MONDO_0012722 seeAlso "https://rarediseases.info.nih.gov/diseases/10568/dauwerse-peters-syndrome" @default.
• MONDO_0012723 seeAlso "https://rarediseases.info.nih.gov/diseases/10487/leber-congenital-amaurosis-10" @default.
• MONDO_0012736 seeAlso "https://rarediseases.info.nih.gov/diseases/10435/long-qt-syndrome-9" @default.
• MONDO_0012737 seeAlso "https://rarediseases.info.nih.gov/diseases/10436/long-qt-syndrome-10" @default.
• MONDO_0012738 seeAlso "https://rarediseases.info.nih.gov/diseases/10437/long-qt-syndrome-11" @default.
• MONDO_0012742 seeAlso "https://rarediseases.info.nih.gov/diseases/10361/brugada-syndrome-3" @default.
• MONDO_0012743 seeAlso "https://rarediseases.info.nih.gov/diseases/10362/brugada-syndrome-4" @default.
• MONDO_0012753 seeAlso "https://rarediseases.info.nih.gov/diseases/10498/amyotrophic-lateral-sclerosis-type-9" @default.
• MONDO_0012756 seeAlso "https://rarediseases.info.nih.gov/diseases/10740/16p112-deletion-syndrome" @default.
• MONDO_0012759 seeAlso "https://rarediseases.info.nih.gov/diseases/10573/camptodactyly-syndrome-guadalajara-type-3" @default.
• MONDO_0012761 seeAlso "https://rarediseases.info.nih.gov/diseases/10360/chromosome-3q29-microduplication-syndrome" @default.
• MONDO_0012789 seeAlso "https://rarediseases.info.nih.gov/diseases/10539/dystonia-16" @default.
• MONDO_0012790 seeAlso "https://rarediseases.info.nih.gov/diseases/10497/amyotrophic-lateral-sclerosis-type-10" @default.
• MONDO_0012791 seeAlso "https://rarediseases.info.nih.gov/diseases/3681/encephalomyopathy" @default.
• MONDO_0012796 seeAlso "https://rarediseases.info.nih.gov/diseases/10379/retinitis-pigmentosa-41" @default.
• MONDO_0012800 seeAlso "https://rarediseases.info.nih.gov/diseases/10373/multiple-familial-trichoepithelioma-2" @default.
• MONDO_0012812 seeAlso "https://rarediseases.info.nih.gov/diseases/12900/early-infantile-epileptic-encephalopathy-4" @default.
• MONDO_0012813 seeAlso "https://rarediseases.info.nih.gov/diseases/10378/retinitis-pigmentosa-29" @default.
• MONDO_0012818 seeAlso "https://rarediseases.info.nih.gov/diseases/10663/maturity-onset-diabetes-of-the-young-type-9" @default.
• MONDO_0012853 seeAlso "https://rarediseases.info.nih.gov/diseases/4497/progeroid-syndrome-petty-type" @default.
• MONDO_0012856 seeAlso "https://rarediseases.info.nih.gov/diseases/10358/birk-barel-syndrome" @default.
• MONDO_0012859 seeAlso "https://rarediseases.info.nih.gov/diseases/10106/osteopetrosis-autosomal-recessive-7" @default.
• MONDO_0012871 seeAlso "https://rarediseases.info.nih.gov/diseases/10364/jervell-and-lange-nielsen-syndrome-2" @default.
• MONDO_0012880 seeAlso "https://rarediseases.info.nih.gov/diseases/10773/kallmann-syndrome-5" @default.
• MONDO_0012897 seeAlso "https://rarediseases.info.nih.gov/diseases/9670/factor-xi-deficiency" @default.
• MONDO_0012901 seeAlso "https://rarediseases.info.nih.gov/diseases/4477/prekallikrein-deficiency-congenital" @default.
• MONDO_0012911 seeAlso "https://rarediseases.info.nih.gov/diseases/10681/pseudohypoparathyroidism-type-1c" @default.
• MONDO_0012912 seeAlso "https://rarediseases.info.nih.gov/diseases/7860/pseudopseudohypoparathyroidism" @default.
• MONDO_0012915 seeAlso "https://rarediseases.info.nih.gov/diseases/10591/chromosome-1q211-duplication-syndrome" @default.
• MONDO_0012923 seeAlso "https://rarediseases.info.nih.gov/diseases/13389/congenital-generalized-lipodystrophy-type-3" @default.
• MONDO_0012927 seeAlso "https://rarediseases.info.nih.gov/diseases/3738/chromosome-1q41-q42-deletion-syndrome" @default.
• MONDO_0012945 seeAlso "https://rarediseases.info.nih.gov/diseases/10496/amyotrophic-lateral-sclerosis-type-11" @default.
• MONDO_0012986 seeAlso "https://rarediseases.info.nih.gov/diseases/10785/bilateral-parasagittal-parieto-occipital-polymicrogyria" @default.
• MONDO_0012988 seeAlso "https://rarediseases.info.nih.gov/diseases/10774/kallmann-syndrome-6" @default.
• MONDO_0012990 seeAlso "https://rarediseases.info.nih.gov/diseases/10882/leber-congenital-amaurosis-13" @default.
• MONDO_0012999 seeAlso "https://rarediseases.info.nih.gov/diseases/2578/guanidinoacetate-methyltransferase-deficiency" @default.
• MONDO_0013000 seeAlso "https://rarediseases.info.nih.gov/diseases/4445/aminolevulinate-dehydratase-deficiency-porphyria" @default.
• MONDO_0013006 seeAlso "https://rarediseases.info.nih.gov/diseases/3919/isolated-growth-hormone-deficiency-type-1b" @default.
• MONDO_0013009 seeAlso "https://rarediseases.info.nih.gov/diseases/10689/megarbane-jalkh-syndrome" @default.
• MONDO_0013014 seeAlso "https://rarediseases.info.nih.gov/diseases/10513/spondyloepimetaphyseal-dysplasia-aggrecan-type" @default.
• MONDO_0013024 seeAlso "https://rarediseases.info.nih.gov/diseases/13124/chronic-thromboembolic-pulmonary-hypertension" @default.
• MONDO_0013035 seeAlso "https://rarediseases.info.nih.gov/diseases/4118/orofaciodigital-syndrome-11" @default.
• MONDO_0013036 seeAlso "https://rarediseases.info.nih.gov/diseases/10582/zechi-ceide-syndrome" @default.
• MONDO_0013047 seeAlso "https://rarediseases.info.nih.gov/diseases/3160/lactate-dehydrogenase-a-deficiency" @default.
• MONDO_0013051 seeAlso "https://rarediseases.info.nih.gov/diseases/1641/cutis-laxa-autosomal-recessive-type-2b" @default.
• MONDO_0013055 seeAlso "https://rarediseases.info.nih.gov/diseases/10683/stargardt-macular-degeneration-absent-or-hypoplastic-corpus-callosum-mental-retardation-and-dysmorphic-features" @default.
• MONDO_0013074 seeAlso "https://rarediseases.info.nih.gov/diseases/2108/encephalocraniocutaneous-lipomatosis" @default.
• MONDO_0013090 seeAlso "https://rarediseases.info.nih.gov/diseases/10592/chromosome-19q1311-deletion-syndrome" @default.
• MONDO_0013099 seeAlso "https://rarediseases.info.nih.gov/diseases/2252/familial-hypopituitarism" @default.
• MONDO_0013171 seeAlso "https://rarediseases.info.nih.gov/diseases/4606/purine-nucleoside-phosphorylase-deficiency" @default.
• MONDO_0013178 seeAlso "https://rarediseases.info.nih.gov/diseases/12585/congenital-muscular-dystrophy-due-to-lmna-mutation" @default.
• MONDO_0013186 seeAlso "https://rarediseases.info.nih.gov/diseases/10701/noonan-syndrome-6" @default.
• MONDO_0013231 seeAlso "https://rarediseases.info.nih.gov/diseases/10883/leber-congenital-amaurosis-14" @default.
• MONDO_0013245 seeAlso "https://rarediseases.info.nih.gov/diseases/10775/itch-e3-ubiquitin-ligase-deficiency" @default.
• MONDO_0013254 seeAlso "https://rarediseases.info.nih.gov/diseases/10933/microcephaly-seizures-and-developmental-delay" @default.
• MONDO_0013262 seeAlso "https://rarediseases.info.nih.gov/diseases/12832/dilated-cardiomyopathy-1s" @default.
• MONDO_0013268 seeAlso "https://rarediseases.info.nih.gov/diseases/12641/frontonasal-dysplasia-with-alopecia-and-genital-anomaly" @default.
• MONDO_0013271 seeAlso "https://rarediseases.info.nih.gov/diseases/12640/frontonasal-dysplasia-severe-microphthalmia-severe-facial-clefting-syndrome" @default.
• MONDO_0013273 seeAlso "https://rarediseases.info.nih.gov/diseases/10755/chromosome-16p133-duplication" @default.
• MONDO_0013276 seeAlso "https://rarediseases.info.nih.gov/diseases/4697/reynolds-syndrome" @default.
• MONDO_0013282 seeAlso "https://rarediseases.info.nih.gov/diseases/5784/alpha-1-antitrypsin-deficiency" @default.
• MONDO_0013301 seeAlso "https://rarediseases.info.nih.gov/diseases/365/aromatase-deficiency" @default.
• MONDO_0013310 seeAlso "https://rarediseases.info.nih.gov/diseases/12664/congenital-adrenal-hyperplasia-due-to-cytochrome-p450-oxidoreductase-deficiency" @default.

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