FRINK Linked Data Fragments server

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

• MONDO_0010930 seeAlso "https://rarediseases.info.nih.gov/diseases/719/anophthalmia-plus-syndrome" @default.
• MONDO_0010932 seeAlso "https://rarediseases.info.nih.gov/diseases/10123/progressive-bifocal-chorioretinal-atrophy" @default.
• MONDO_0010945 seeAlso "https://rarediseases.info.nih.gov/diseases/10387/retinitis-pigmentosa-17" @default.
• MONDO_0010947 seeAlso "https://rarediseases.info.nih.gov/diseases/5968/budd-chiari-syndrome" @default.
• MONDO_0010949 seeAlso "https://rarediseases.info.nih.gov/diseases/9192/charcot-marie-tooth-disease-type-2b" @default.
• MONDO_0010964 seeAlso "https://rarediseases.info.nih.gov/diseases/9792/multiple-epiphyseal-dysplasia-3" @default.
• MONDO_0010968 seeAlso "https://rarediseases.info.nih.gov/diseases/2490/glaucoma-3-primary-infantile-b" @default.
• MONDO_0010969 seeAlso "https://rarediseases.info.nih.gov/diseases/10655/cone-rod-dystrophy-5" @default.
• MONDO_0010977 seeAlso "https://rarediseases.info.nih.gov/diseases/9158/brody-myopathy" @default.
• MONDO_0010979 seeAlso "https://rarediseases.info.nih.gov/diseases/9294/timothy-syndrome" @default.
• MONDO_0010981 seeAlso "https://rarediseases.info.nih.gov/diseases/5210/tibia-absent-polydactyly-arachnoid-cyst" @default.
• MONDO_0010984 seeAlso "https://rarediseases.info.nih.gov/diseases/5438/usher-syndrome-type-1d" @default.
• MONDO_0010988 seeAlso "https://rarediseases.info.nih.gov/diseases/756/aplasia-cutis-myopia" @default.
• MONDO_0010995 seeAlso "https://rarediseases.info.nih.gov/diseases/1247/charcot-marie-tooth-disease-type-1c" @default.
• MONDO_0010996 seeAlso "https://rarediseases.info.nih.gov/diseases/9902/hereditary-hemorrhagic-telangiectasia-type-3" @default.
• MONDO_0011003 seeAlso "https://rarediseases.info.nih.gov/diseases/5644/cardiomyopathy-dilated-with-conduction-defect-type-2" @default.
• MONDO_0011007 seeAlso "https://rarediseases.info.nih.gov/diseases/2397/froster-huch-syndrome" @default.
• MONDO_0011017 seeAlso "https://rarediseases.info.nih.gov/diseases/9795/naxos-disease" @default.
• MONDO_0011020 seeAlso "https://rarediseases.info.nih.gov/diseases/404/osteoporosis-oculocutaneous-hypopigmentation-syndrome" @default.
• MONDO_0011024 seeAlso "https://rarediseases.info.nih.gov/diseases/1917/dermatitis-herpetiformis" @default.
• MONDO_0011028 seeAlso "https://rarediseases.info.nih.gov/diseases/8573/limb-girdle-muscular-dystrophy-type-2f" @default.
• MONDO_0011034 seeAlso "https://rarediseases.info.nih.gov/diseases/4053/odontomicronychial-dysplasia" @default.
• MONDO_0011035 seeAlso "https://rarediseases.info.nih.gov/diseases/372/neurofibromatosis-noonan-syndrome" @default.
• MONDO_0011041 seeAlso "https://rarediseases.info.nih.gov/diseases/10526/ectodermal-dysplasia-with-natal-teeth-turnpenny-type" @default.
• MONDO_0011049 seeAlso "https://rarediseases.info.nih.gov/diseases/958/fine-lubinsky-syndrome" @default.
• MONDO_0011051 seeAlso "https://rarediseases.info.nih.gov/diseases/4827/lethal-short-limb-skeletal-dysplasia-al-gazali-type" @default.
• MONDO_0011052 seeAlso "https://rarediseases.info.nih.gov/diseases/641/amelia-cleft-lip-palate-hydrocephalus-iris-coloboma" @default.
• MONDO_0011063 seeAlso "https://rarediseases.info.nih.gov/diseases/2682/ectodermal-dysplasia-hidrotic-christianson-fourie-type" @default.
• MONDO_0011064 seeAlso "https://rarediseases.info.nih.gov/diseases/3226/lethal-chondrodysplasia-seller-type" @default.
• MONDO_0011066 seeAlso "https://rarediseases.info.nih.gov/diseases/1253/charcot-marie-tooth-disease-type-4b1" @default.
• MONDO_0011069 seeAlso "https://rarediseases.info.nih.gov/diseases/1227/cervical-ribs-sprengel-anomaly-anal-atresia-and-urethral-obstruction" @default.
• MONDO_0011075 seeAlso "https://rarediseases.info.nih.gov/diseases/10392/retinitis-pigmentosa-18" @default.
• MONDO_0011077 seeAlso "https://rarediseases.info.nih.gov/diseases/3614/microcephaly-corpus-callosum-dysgenesis-and-cleft-lip-palate" @default.
• MONDO_0011079 seeAlso "https://rarediseases.info.nih.gov/diseases/4703/rhizomelic-dysplasia-patterson-lowry-type" @default.
• MONDO_0011080 seeAlso "https://rarediseases.info.nih.gov/diseases/5170/progressive-deafness-with-stapes-fixation" @default.
• MONDO_0011081 seeAlso "https://rarediseases.info.nih.gov/diseases/1428/collins-pope-syndrome" @default.
• MONDO_0011082 seeAlso "https://rarediseases.info.nih.gov/diseases/4031/oculoauriculofrontonasal-syndrome" @default.
• MONDO_0011083 seeAlso "https://rarediseases.info.nih.gov/diseases/265/trichodental-syndrome" @default.
• MONDO_0011085 seeAlso "https://rarediseases.info.nih.gov/diseases/3973/charcot-marie-tooth-disease-type-4d" @default.
• MONDO_0011089 seeAlso "https://rarediseases.info.nih.gov/diseases/10483/patent-ductus-venosus" @default.
• MONDO_0011090 seeAlso "https://rarediseases.info.nih.gov/diseases/8583/hereditary-congenital-facial-paresis" @default.
• MONDO_0011091 seeAlso "https://rarediseases.info.nih.gov/diseases/1251/charcot-marie-tooth-disease-type-2d" @default.
• MONDO_0011092 seeAlso "https://rarediseases.info.nih.gov/diseases/8494/ribbing-disease" @default.
• MONDO_0011110 seeAlso "https://rarediseases.info.nih.gov/diseases/2025/dyssegmental-dysplasia-and-glaucoma" @default.
• MONDO_0011113 seeAlso "https://rarediseases.info.nih.gov/diseases/9201/charcot-marie-tooth-disease-type-4c" @default.
• MONDO_0011116 seeAlso "https://rarediseases.info.nih.gov/diseases/3378/manouvrier-syndrome" @default.
• MONDO_0011121 seeAlso "https://rarediseases.info.nih.gov/diseases/10544/paragangliomas-2" @default.
• MONDO_0011129 seeAlso "https://rarediseases.info.nih.gov/diseases/2484/glaucoma-type-1c" @default.
• MONDO_0011130 seeAlso "https://rarediseases.info.nih.gov/diseases/10031/sebaceous-gland-hyperplasia-familial-presenile" @default.
• MONDO_0011132 seeAlso "https://rarediseases.info.nih.gov/diseases/4358/t-cell-immunodeficiency-congenital-alopecia-and-nail-dystrophy" @default.
• MONDO_0011134 seeAlso "https://rarediseases.info.nih.gov/diseases/5584/curry-jones-syndrome" @default.
• MONDO_0011136 seeAlso "https://rarediseases.info.nih.gov/diseases/8345/quebec-platelet-disorder" @default.
• MONDO_0011137 seeAlso "https://rarediseases.info.nih.gov/diseases/10398/retinitis-pigmentosa-19" @default.
• MONDO_0011142 seeAlso "https://rarediseases.info.nih.gov/diseases/545/adducted-thumbs-dundar-type" @default.
• MONDO_0011144 seeAlso "https://rarediseases.info.nih.gov/diseases/1224/neuronal-ceroid-lipofuscinosis-6" @default.
• MONDO_0011148 seeAlso "https://rarediseases.info.nih.gov/diseases/10571/spondylospinal-thoracic-dysostosis" @default.
• MONDO_0011153 seeAlso "https://rarediseases.info.nih.gov/diseases/9927/hyperinsulinemic-hypoglycemia-familial-2" @default.
• MONDO_0011156 seeAlso "https://rarediseases.info.nih.gov/diseases/1288/progressive-familial-intrahepatic-cholestasis-type-2" @default.
• MONDO_0011157 seeAlso "https://rarediseases.info.nih.gov/diseases/229/gomez-lopez-hernandez-syndrome" @default.
• MONDO_0011163 seeAlso "https://rarediseases.info.nih.gov/diseases/3367/malignant-hyperthermia-susceptibility-type-5" @default.
• MONDO_0011164 seeAlso "https://rarediseases.info.nih.gov/diseases/3368/malignant-hyperthermia-susceptibility-type-6" @default.
• MONDO_0011166 seeAlso "https://rarediseases.info.nih.gov/diseases/284/irons-bhan-syndrome" @default.
• MONDO_0011185 seeAlso "https://rarediseases.info.nih.gov/diseases/9275/corneal-dystrophy-thiel-behnke-type" @default.
• MONDO_0011186 seeAlso "https://rarediseases.info.nih.gov/diseases/10043/usher-syndrome-type-1f" @default.
• MONDO_0011195 seeAlso "https://rarediseases.info.nih.gov/diseases/5439/usher-syndrome-type-1e" @default.
• MONDO_0011196 seeAlso "https://rarediseases.info.nih.gov/diseases/10503/amyotrophic-lateral-sclerosis-type-5" @default.
• MONDO_0011198 seeAlso "https://rarediseases.info.nih.gov/diseases/10618/spondyloepimetaphyseal-dysplasia-missouri-type" @default.
• MONDO_0011203 seeAlso "https://rarediseases.info.nih.gov/diseases/10090/pierre-robin-sequence-with-pectus-excavatum-and-rib-and-scapular-anomalies" @default.
• MONDO_0011205 seeAlso "https://rarediseases.info.nih.gov/diseases/10329/medium-chain-3-ketoacyl-coa-thiolase-deficiency" @default.
• MONDO_0011211 seeAlso "https://rarediseases.info.nih.gov/diseases/8720/axial-spondylometaphyseal-dysplasia" @default.
• MONDO_0011214 seeAlso "https://rarediseases.info.nih.gov/diseases/1289/progressive-familial-intrahepatic-cholestasis-type-3" @default.
• MONDO_0011217 seeAlso "https://rarediseases.info.nih.gov/diseases/10283/desmosterolosis" @default.
• MONDO_0011221 seeAlso "https://rarediseases.info.nih.gov/diseases/10178/weyers-ulnar-rayoligodactyly-syndrome" @default.
• MONDO_0011223 seeAlso "https://rarediseases.info.nih.gov/diseases/10502/amyotrophic-lateral-sclerosis-type-4" @default.
• MONDO_0011224 seeAlso "https://rarediseases.info.nih.gov/diseases/9697/monomelic-amyotrophy" @default.
• MONDO_0011225 seeAlso "https://rarediseases.info.nih.gov/diseases/9987/severe-combined-immunodeficiency-with-sensitivity-to-ionizing-radiation" @default.
• MONDO_0011229 seeAlso "https://rarediseases.info.nih.gov/diseases/2198/ethylmalonic-encephalopathy" @default.
• MONDO_0011236 seeAlso "https://rarediseases.info.nih.gov/diseases/9930/hyperinsulinemic-hypoglycemia-familial-3" @default.
• MONDO_0011244 seeAlso "https://rarediseases.info.nih.gov/diseases/6985/marshall-smith-syndrome" @default.
• MONDO_0011246 seeAlso "https://rarediseases.info.nih.gov/diseases/10317/muscular-dystrophy-congenital-megaconial-type" @default.
• MONDO_0011247 seeAlso "https://rarediseases.info.nih.gov/diseases/9985/jejunal-atresia-with-renal-adysplasia" @default.
• MONDO_0011252 seeAlso "https://rarediseases.info.nih.gov/diseases/4980/spondyloepimetaphyseal-dysplasia-shohat-type" @default.
• MONDO_0011253 seeAlso "https://rarediseases.info.nih.gov/diseases/1583/craniomicromelic-syndrome" @default.
• MONDO_0011259 seeAlso "https://rarediseases.info.nih.gov/diseases/10393/retinitis-pigmentosa-22" @default.
• MONDO_0011266 seeAlso "https://rarediseases.info.nih.gov/diseases/9728/myotonic-dystrophy-type-2" @default.
• MONDO_0011272 seeAlso "https://rarediseases.info.nih.gov/diseases/10384/retinitis-pigmentosa-25" @default.
• MONDO_0011273 seeAlso "https://rarediseases.info.nih.gov/diseases/581/asrar-facharzt-haque-syndrome" @default.
• MONDO_0011274 seeAlso "https://rarediseases.info.nih.gov/diseases/7097/muenke-syndrome" @default.
• MONDO_0011275 seeAlso "https://rarediseases.info.nih.gov/diseases/507/acromesomelic-dysplasia-maroteaux-type" @default.
• MONDO_0011296 seeAlso "https://rarediseases.info.nih.gov/diseases/8743/meckel-syndrome-type-2" @default.
• MONDO_0011301 seeAlso "https://rarediseases.info.nih.gov/diseases/10680/pseudohypoparathyroidism-type-1b" @default.
• MONDO_0011312 seeAlso "https://rarediseases.info.nih.gov/diseases/8488/nonmedullary-thyroid-carcinoma-with-or-without-cell-oxyphilia" @default.
• MONDO_0011318 seeAlso "https://rarediseases.info.nih.gov/diseases/10219/tonoki-syndrome" @default.
• MONDO_0011326 seeAlso "https://rarediseases.info.nih.gov/diseases/10215/adult-onset-citrullinemia-type-ii" @default.
• MONDO_0011327 seeAlso "https://rarediseases.info.nih.gov/diseases/3971/neuronal-intranuclear-inclusion-disease" @default.
• MONDO_0011331 seeAlso "https://rarediseases.info.nih.gov/diseases/10156/chylothorax-congenital" @default.
• MONDO_0011335 seeAlso "https://rarediseases.info.nih.gov/diseases/9866/spondyloepimetaphyseal-dysplasia-with-multiple-dislocations" @default.
• MONDO_0011336 seeAlso "https://rarediseases.info.nih.gov/diseases/9929/hemophagocytic-lymphohistiocytosis-familial-4" @default.
• MONDO_0011337 seeAlso "https://rarediseases.info.nih.gov/diseases/9922/hemophagocytic-lymphohistiocytosis-familial-2" @default.
• MONDO_0011338 seeAlso "https://rarediseases.info.nih.gov/diseases/8198/omenn-syndrome" @default.

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