FRINK Linked Data Fragments server

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

• MONDO_0013325 seeAlso "https://rarediseases.info.nih.gov/diseases/1173/cdg-syndrome-type-3" @default.
• MONDO_0013327 seeAlso "https://rarediseases.info.nih.gov/diseases/10738/primary-hyperoxaluria-type-3" @default.
• MONDO_0013343 seeAlso "https://rarediseases.info.nih.gov/diseases/12958/c1q-deficiency" @default.
• MONDO_0013352 seeAlso "https://rarediseases.info.nih.gov/diseases/12501/intellectual-disability-severe-speech-delay-mild-dysmorphism-syndrome" @default.
• MONDO_0013357 seeAlso "https://rarediseases.info.nih.gov/diseases/5408/chromosome-17q112-deletion-syndrome" @default.
• MONDO_0013361 seeAlso "https://rarediseases.info.nih.gov/diseases/2235/factor-2-deficiency" @default.
• MONDO_0013367 seeAlso "https://rarediseases.info.nih.gov/diseases/3285/long-qt-syndrome-2" @default.
• MONDO_0013370 seeAlso "https://rarediseases.info.nih.gov/diseases/10434/long-qt-syndrome-6" @default.
• MONDO_0013372 seeAlso "https://rarediseases.info.nih.gov/diseases/10433/long-qt-syndrome-5" @default.
• MONDO_0013383 seeAlso "https://rarediseases.info.nih.gov/diseases/2699/hirschsprung-disease-type-3" @default.
• MONDO_0013389 seeAlso "https://rarediseases.info.nih.gov/diseases/13318/early-infantile-epileptic-encephalopathy-12" @default.
• MONDO_0013395 seeAlso "https://rarediseases.info.nih.gov/diseases/10405/retinitis-pigmentosa-4" @default.
• MONDO_0013421 seeAlso "https://rarediseases.info.nih.gov/diseases/10625/complement-component-8-deficiency-type-2" @default.
• MONDO_0013422 seeAlso "https://rarediseases.info.nih.gov/diseases/10626/complement-component-8-deficiency-type-1" @default.
• MONDO_0013425 seeAlso "https://rarediseases.info.nih.gov/diseases/10404/retinitis-pigmentosa-20" @default.
• MONDO_0013446 seeAlso "https://rarediseases.info.nih.gov/diseases/10490/leber-congenital-amaurosis-6" @default.
• MONDO_0013449 seeAlso "https://rarediseases.info.nih.gov/diseases/10880/leber-congenital-amaurosis-7" @default.
• MONDO_0013452 seeAlso "https://rarediseases.info.nih.gov/diseases/12811/multisystemic-smooth-muscle-dysfunction-syndrome" @default.
• MONDO_0013453 seeAlso "https://rarediseases.info.nih.gov/diseases/10881/leber-congenital-amaurosis-8" @default.
• MONDO_0013454 seeAlso "https://rarediseases.info.nih.gov/diseases/10488/leber-congenital-amaurosis-11" @default.
• MONDO_0013457 seeAlso "https://rarediseases.info.nih.gov/diseases/10884/leber-congenital-amaurosis-15" @default.
• MONDO_0013480 seeAlso "https://rarediseases.info.nih.gov/diseases/12155/renal-hypomagnesemia-6" @default.
• MONDO_0013523 seeAlso "https://rarediseases.info.nih.gov/diseases/11008/nestor-guillermo-progeria-syndrome" @default.
• MONDO_0013540 seeAlso "https://rarediseases.info.nih.gov/diseases/13030/deafness-lymphedema-leukemia-syndrome" @default.
• MONDO_0013548 seeAlso "https://rarediseases.info.nih.gov/diseases/9154/acetyl-coa-acetyltransferase-2-deficiency" @default.
• MONDO_0013587 seeAlso "https://rarediseases.info.nih.gov/diseases/3161/lactate-dehydrogenase-b-deficiency" @default.
• MONDO_0013591 seeAlso "https://rarediseases.info.nih.gov/diseases/13376/multiple-epiphyseal-dysplasia-6" @default.
• MONDO_0013598 seeAlso "https://rarediseases.info.nih.gov/diseases/10238/myostatin-related-muscle-hypertrophy" @default.
• MONDO_0013613 seeAlso "https://rarediseases.info.nih.gov/diseases/10885/leber-congenital-amaurosis-16" @default.
• MONDO_0013688 seeAlso "https://rarediseases.info.nih.gov/diseases/11004/linear-and-whorled-nevoid-hypermelanosis" @default.
• MONDO_0013753 seeAlso "https://rarediseases.info.nih.gov/diseases/12435/charcot-marie-tooth-disease-type-2p" @default.
• MONDO_0013762 seeAlso "https://rarediseases.info.nih.gov/diseases/12678/lipoic-acid-synthetase-deficiency" @default.
• MONDO_0013802 seeAlso "https://rarediseases.info.nih.gov/diseases/13264/infantile-cerebellar-retinal-degeneration" @default.
• MONDO_0013808 seeAlso "https://rarediseases.info.nih.gov/diseases/6958/maffucci-syndrome" @default.
• MONDO_0013858 seeAlso "https://rarediseases.info.nih.gov/diseases/10919/pontine-tegmental-cap-dysplasia" @default.
• MONDO_0013867 seeAlso "https://rarediseases.info.nih.gov/diseases/12861/brown-vialetto-van-laere-syndrome-2" @default.
• MONDO_0013869 seeAlso "https://rarediseases.info.nih.gov/diseases/10666/dihydroxyadeninuria" @default.
• MONDO_0013873 seeAlso "https://rarediseases.info.nih.gov/diseases/12312/image-syndrome" @default.
• MONDO_0013898 seeAlso "https://rarediseases.info.nih.gov/diseases/11003/karyomegalic-interstitial-nephritis" @default.
• MONDO_0013907 seeAlso "https://rarediseases.info.nih.gov/diseases/10786/bilateral-generalized-polymicrogyria" @default.
• MONDO_0013914 seeAlso "https://rarediseases.info.nih.gov/diseases/276/eunuchoidism-familial-hypogonadotropic" @default.
• MONDO_0013925 seeAlso "https://rarediseases.info.nih.gov/diseases/12621/methylmalonic-acidemia-with-homocystinuria-type-cblj" @default.
• MONDO_0013959 seeAlso "https://rarediseases.info.nih.gov/diseases/12441/charcot-marie-tooth-disease-type-4f" @default.
• MONDO_0013965 seeAlso "https://rarediseases.info.nih.gov/diseases/12645/lethal-congenital-contracture-syndrome-4" @default.
• MONDO_0013991 seeAlso "https://rarediseases.info.nih.gov/diseases/13015/obesity-due-to-congenital-leptin-deficiency" @default.
• MONDO_0014028 seeAlso "https://rarediseases.info.nih.gov/diseases/13059/distal-arthrogryposis-type-5d" @default.
• MONDO_0014035 seeAlso "https://rarediseases.info.nih.gov/diseases/3505/severe-intellectual-disability-progressive-spastic-diplegia-syndrome" @default.
• MONDO_0014096 seeAlso "https://rarediseases.info.nih.gov/diseases/3498/microcephaly-intellectual-disability-phalangeal-and-neurological-anomalies-syndrome" @default.
• MONDO_0014208 seeAlso "https://rarediseases.info.nih.gov/diseases/12451/charcot-marie-tooth-disease-type-2r" @default.
• MONDO_0014220 seeAlso "https://rarediseases.info.nih.gov/diseases/547/adenosine-monophosphate-deaminase-1-deficiency" @default.
• MONDO_0014221 seeAlso "https://rarediseases.info.nih.gov/diseases/5287/triosephosphate-isomerase-deficiency" @default.
• MONDO_0014229 seeAlso "https://rarediseases.info.nih.gov/diseases/13235/syndromic-microphthalmia-12" @default.
• MONDO_0014244 seeAlso "https://rarediseases.info.nih.gov/diseases/12732/hereditary-sensory-and-autonomic-neuropathy-type-7" @default.
• MONDO_0014262 seeAlso "https://rarediseases.info.nih.gov/diseases/12356/rienhoff-syndrome" @default.
• MONDO_0014276 seeAlso "https://rarediseases.info.nih.gov/diseases/9521/cd3-deficiency" @default.
• MONDO_0014392 seeAlso "https://rarediseases.info.nih.gov/diseases/12901/early-infantile-epileptic-encephalopathy-25" @default.
• MONDO_0014405 seeAlso "https://rarediseases.info.nih.gov/diseases/12357/sting-associated-vasculopathy-with-onset-in-infancy" @default.
• MONDO_0014421 seeAlso "https://rarediseases.info.nih.gov/diseases/2499/glucocorticoid-resistance" @default.
• MONDO_0014431 seeAlso "https://rarediseases.info.nih.gov/diseases/13126/lipe-related-familial-partial-lipodystrophy" @default.
• MONDO_0014433 seeAlso "https://rarediseases.info.nih.gov/diseases/823/bardet-biedl-syndrome-4" @default.
• MONDO_0014434 seeAlso "https://rarediseases.info.nih.gov/diseases/10204/bardet-biedl-syndrome-5" @default.
• MONDO_0014435 seeAlso "https://rarediseases.info.nih.gov/diseases/10206/bardet-biedl-syndrome-7" @default.
• MONDO_0014436 seeAlso "https://rarediseases.info.nih.gov/diseases/10207/bardet-biedl-syndrome-8" @default.
• MONDO_0014437 seeAlso "https://rarediseases.info.nih.gov/diseases/10208/bardet-biedl-syndrome-9" @default.
• MONDO_0014449 seeAlso "https://rarediseases.info.nih.gov/diseases/13056/congenital-analbuminemia" @default.
• MONDO_0014452 seeAlso "https://rarediseases.info.nih.gov/diseases/2004/dysfibrinogenemia" @default.
• MONDO_0014477 seeAlso "https://rarediseases.info.nih.gov/diseases/12391/early-infantile-epileptic-encephalopathy-26" @default.
• MONDO_0014493 seeAlso "https://rarediseases.info.nih.gov/diseases/12316/autoimmune-lymphoproliferative-syndrome-due-to-ctla4-haploinsuffiency" @default.
• MONDO_0014507 seeAlso "https://rarediseases.info.nih.gov/diseases/28/catel-manzke-syndrome" @default.
• MONDO_0014557 seeAlso "https://rarediseases.info.nih.gov/diseases/13111/ataxia-oculomotor-apraxia-type-4" @default.
• MONDO_0014637 seeAlso "https://rarediseases.info.nih.gov/diseases/12653/dock2-deficiency" @default.
• MONDO_0014658 seeAlso saddan @default.
• MONDO_0014708 seeAlso "https://rarediseases.info.nih.gov/diseases/6072/ring-chromosome-14" @default.
• MONDO_0014722 seeAlso "https://rarediseases.info.nih.gov/diseases/9163/roifman-syndrome" @default.
• MONDO_0014880 seeAlso "https://rarediseases.info.nih.gov/diseases/10691/duane-syndrome-type-3" @default.
• MONDO_0014912 seeAlso "https://rarediseases.info.nih.gov/diseases/13198/otulipenia" @default.
• MONDO_0015028 seeAlso "https://rarediseases.info.nih.gov/diseases/5677/48xxyy-syndrome" @default.
• MONDO_0015032 seeAlso "https://rarediseases.info.nih.gov/diseases/10921/intraneural-perineurioma" @default.
• MONDO_0015059 seeAlso "https://rarediseases.info.nih.gov/diseases/10793/progressive-non-fluent-aphasia" @default.
• MONDO_0015086 seeAlso "https://rarediseases.info.nih.gov/diseases/853/benallegue-lacete-syndrome" @default.
• MONDO_0015094 seeAlso "https://rarediseases.info.nih.gov/diseases/5050/subependymal-nodular-heterotopia" @default.
• MONDO_0015096 seeAlso "https://rarediseases.info.nih.gov/diseases/2887/hypofibrinogenemia-familial" @default.
• MONDO_0015177 seeAlso "https://rarediseases.info.nih.gov/diseases/3562/metaphyseal-anadysplasia" @default.
• MONDO_0015183 seeAlso "https://rarediseases.info.nih.gov/diseases/1502/short-bowel-syndrome" @default.
• MONDO_0015196 seeAlso "https://rarediseases.info.nih.gov/diseases/5467/vein-of-galen-aneurysm" @default.
• MONDO_0015197 seeAlso "https://rarediseases.info.nih.gov/diseases/670/aneurysm-of-sinus-of-valsalva" @default.
• MONDO_0015200 seeAlso "https://rarediseases.info.nih.gov/diseases/693/anisakiasis" @default.
• MONDO_0015230 seeAlso "https://rarediseases.info.nih.gov/diseases/717/anophthalmia-megalocornea-cardiopathy-skeletal-anomalies" @default.
• MONDO_0015231 seeAlso "https://rarediseases.info.nih.gov/diseases/5893/bartter-syndrome" @default.
• MONDO_0015233 seeAlso "https://rarediseases.info.nih.gov/diseases/1163/caudal-appendage-deafness" @default.
• MONDO_0015236 seeAlso "https://rarediseases.info.nih.gov/diseases/741/aortic-arches-defect" @default.
• MONDO_0015237 seeAlso "https://rarediseases.info.nih.gov/diseases/364/arrhinia" @default.
• MONDO_0015238 seeAlso "https://rarediseases.info.nih.gov/diseases/8755/arhinia-choanal-atresia-microphthalmia" @default.
• MONDO_0015240 seeAlso "https://rarediseases.info.nih.gov/diseases/787/distal-arthrogryposis-type-1" @default.
• MONDO_0015241 seeAlso "https://rarediseases.info.nih.gov/diseases/783/arthrogryposis-like-disorder" @default.
• MONDO_0015243 seeAlso "https://rarediseases.info.nih.gov/diseases/602/allergic-bronchopulmonary-aspergillosis" @default.
• MONDO_0015250 seeAlso "https://rarediseases.info.nih.gov/diseases/4942/spinal-atrophy-ophthalmoplegia-pyramidal-syndrome" @default.
• MONDO_0015252 seeAlso "https://rarediseases.info.nih.gov/diseases/3482/intellectual-disability---athetosis---microphthalmia" @default.
• MONDO_0015259 seeAlso "https://rarediseases.info.nih.gov/diseases/5036/brachydactyly-mesomelia-intellectual-disability-heart-defects-syndrome" @default.
• MONDO_0015261 seeAlso "https://rarediseases.info.nih.gov/diseases/4536/pseudopelade-of-brocq" @default.

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