FRINK Linked Data Fragments server

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

• MONDO_0011872 seeAlso "https://rarediseases.info.nih.gov/diseases/4483/griscelli-syndrome-type-2" @default.
• MONDO_0011873 seeAlso "https://rarediseases.info.nih.gov/diseases/3992/niemann-pick-disease-type-c2" @default.
• MONDO_0011881 seeAlso "https://rarediseases.info.nih.gov/diseases/9173/keratosis-palmoplantaris-striata-3" @default.
• MONDO_0011882 seeAlso "https://rarediseases.info.nih.gov/diseases/5231/skin-fragility-woolly-hair-palmoplantar-keratoderma-syndrome" @default.
• MONDO_0011883 seeAlso "https://rarediseases.info.nih.gov/diseases/10163/curly-hair-acral-keratoderma-caries-syndrome" @default.
• MONDO_0011889 seeAlso "https://rarediseases.info.nih.gov/diseases/9197/charcot-marie-tooth-disease-type-2i" @default.
• MONDO_0011890 seeAlso "https://rarediseases.info.nih.gov/diseases/9189/charcot-marie-tooth-disease-type-1d" @default.
• MONDO_0011894 seeAlso "https://rarediseases.info.nih.gov/diseases/9193/charcot-marie-tooth-disease-type-2e" @default.
• MONDO_0011902 seeAlso "https://rarediseases.info.nih.gov/diseases/9191/charcot-marie-tooth-disease-type-1f" @default.
• MONDO_0011903 seeAlso "https://rarediseases.info.nih.gov/diseases/9198/charcot-marie-tooth-disease-type-2j" @default.
• MONDO_0011907 seeAlso "https://rarediseases.info.nih.gov/diseases/10605/acrocapitofemoral-dysplasia" @default.
• MONDO_0011928 seeAlso "https://rarediseases.info.nih.gov/diseases/1164/caudal-duplication" @default.
• MONDO_0011929 seeAlso "https://rarediseases.info.nih.gov/diseases/6082/chromosome-1p36-deletion-syndrome" @default.
• MONDO_0011934 seeAlso "https://rarediseases.info.nih.gov/diseases/9569/dermatofibrosarcoma-protuberans" @default.
• MONDO_0011939 seeAlso "https://rarediseases.info.nih.gov/diseases/4978/spondyloenchondrodysplasia" @default.
• MONDO_0011945 seeAlso "https://rarediseases.info.nih.gov/diseases/10675/gaucher-disease-perinatal-lethal" @default.
• MONDO_0011948 seeAlso "https://rarediseases.info.nih.gov/diseases/10708/pontocerebellar-hypoplasia-type-3" @default.
• MONDO_0011949 seeAlso "https://rarediseases.info.nih.gov/diseases/3557/thai-symphalangism-syndrome" @default.
• MONDO_0011951 seeAlso "https://rarediseases.info.nih.gov/diseases/9874/amyotrophic-lateral-sclerosis-type-6" @default.
• MONDO_0011952 seeAlso "https://rarediseases.info.nih.gov/diseases/10500/amyotrophic-lateral-sclerosis-type-7" @default.
• MONDO_0011963 seeAlso "https://rarediseases.info.nih.gov/diseases/10167/joubert-syndrome-2" @default.
• MONDO_0011971 seeAlso "https://rarediseases.info.nih.gov/diseases/10581/immunodeficiency-with-hyper-igm-type-5" @default.
• MONDO_0011974 seeAlso "https://rarediseases.info.nih.gov/diseases/10386/retinitis-pigmentosa-7" @default.
• MONDO_0011975 seeAlso "https://rarediseases.info.nih.gov/diseases/5409/uniparental-disomy-paternal-chromosome-14" @default.
• MONDO_0011985 seeAlso "https://rarediseases.info.nih.gov/diseases/10580/immunodeficiency-with-hyper-igm-type-4" @default.
• MONDO_0011997 seeAlso "https://rarediseases.info.nih.gov/diseases/9435/hermansky-pudlak-syndrome-2" @default.
• MONDO_0012008 seeAlso "https://rarediseases.info.nih.gov/diseases/10367/lelis-syndrome" @default.
• MONDO_0012016 seeAlso "https://rarediseases.info.nih.gov/diseases/11904/capillary-malformation-arteriovenous-malformation-syndrome" @default.
• MONDO_0012020 seeAlso "https://rarediseases.info.nih.gov/diseases/10557/22q112-duplication-syndrome" @default.
• MONDO_0012024 seeAlso "https://rarediseases.info.nih.gov/diseases/10397/retinitis-pigmentosa-26" @default.
• MONDO_0012033 seeAlso "https://rarediseases.info.nih.gov/diseases/12299/bradyopsia" @default.
• MONDO_0012041 seeAlso "https://rarediseases.info.nih.gov/diseases/10805/myh-associated-polyposis" @default.
• MONDO_0012044 seeAlso "https://rarediseases.info.nih.gov/diseases/10320/lattice-corneal-dystrophy-type-3a" @default.
• MONDO_0012056 seeAlso "https://rarediseases.info.nih.gov/diseases/9491/leber-congenital-amaurosis-9" @default.
• MONDO_0012064 seeAlso "https://rarediseases.info.nih.gov/diseases/10041/choanal-atresia-hearing-loss-cardiac-defects-craniofacial-dysmorphism-syndrome" @default.
• MONDO_0012074 seeAlso "https://rarediseases.info.nih.gov/diseases/9989/mandibuloacral-dysplasia-with-type-b-lipodystrophy" @default.
• MONDO_0012077 seeAlso "https://rarediseases.info.nih.gov/diseases/10499/amyotrophic-lateral-sclerosis-type-8" @default.
• MONDO_0012084 seeAlso "https://rarediseases.info.nih.gov/diseases/770/aromatic-l-amino-acid-decarboxylase-deficiency" @default.
• MONDO_0012089 seeAlso "https://rarediseases.info.nih.gov/diseases/9886/ichthyosis-prematurity-syndrome" @default.
• MONDO_0012120 seeAlso "https://rarediseases.info.nih.gov/diseases/9888/pyruvate-dehydrogenase-phosphatase-deficiency" @default.
• MONDO_0012126 seeAlso "https://rarediseases.info.nih.gov/diseases/10914/familial-avascular-necrosis-of-the-femoral-head" @default.
• MONDO_0012129 seeAlso "https://rarediseases.info.nih.gov/diseases/10065/leukoencephalopathy-arthritis-colitis-and-hypogammaglobulinema" @default.
• MONDO_0012131 seeAlso "https://rarediseases.info.nih.gov/diseases/10066/metaphyseal-undermodeling-spondylar-dysplasia-and-overgrowth" @default.
• MONDO_0012133 seeAlso "https://rarediseases.info.nih.gov/diseases/10067/lateral-semicircular-canal-malformation-familial-with-external-and-middle-ear-abnormalities" @default.
• MONDO_0012146 seeAlso "https://rarediseases.info.nih.gov/diseases/9928/hemophagocytic-lymphohistiocytosis-familial-3" @default.
• MONDO_0012154 seeAlso "https://rarediseases.info.nih.gov/diseases/9937/myopia-6" @default.
• MONDO_0012172 seeAlso "https://rarediseases.info.nih.gov/diseases/3684/mitochondrial-trifunctional-protein-deficiency" @default.
• MONDO_0012176 seeAlso "https://rarediseases.info.nih.gov/diseases/9835/emanuel-syndrome" @default.
• MONDO_0012184 seeAlso "https://rarediseases.info.nih.gov/diseases/9420/pierson-syndrome" @default.
• MONDO_0012185 seeAlso "https://rarediseases.info.nih.gov/diseases/458/spondylometaphyseal-dysplasia-type-a4" @default.
• MONDO_0012188 seeAlso "https://rarediseases.info.nih.gov/diseases/6618/neuronal-ceroid-lipofuscinosis-9" @default.
• MONDO_0012206 seeAlso "https://rarediseases.info.nih.gov/diseases/10220/czech-dysplasia-metatarsal-type" @default.
• MONDO_0012207 seeAlso "https://rarediseases.info.nih.gov/diseases/9490/flat-umbilicus-familial" @default.
• MONDO_0012215 seeAlso "https://rarediseases.info.nih.gov/diseases/10229/limb-girdle-muscular-dystrophy-type-1a" @default.
• MONDO_0012215 seeAlso "https://rarediseases.info.nih.gov/diseases/8711/spheroid-body-myopathy" @default.
• MONDO_0012220 seeAlso "https://rarediseases.info.nih.gov/diseases/9715/griscelli-syndrome-type-3" @default.
• MONDO_0012235 seeAlso "https://rarediseases.info.nih.gov/diseases/12232/spinocerebellar-ataxia-autosomal-recessive-7" @default.
• MONDO_0012250 seeAlso "https://rarediseases.info.nih.gov/diseases/12442/charcot-marie-tooth-disease-type-4h" @default.
• MONDO_0012259 seeAlso "https://rarediseases.info.nih.gov/diseases/9878/colloid-cysts-of-third-ventricle" @default.
• MONDO_0012272 seeAlso "https://rarediseases.info.nih.gov/diseases/10064/mental-retardation-keratoconus-febrile-seizures-and-sinoatrial-block" @default.
• MONDO_0012274 seeAlso "https://rarediseases.info.nih.gov/diseases/10077/chondrodysplasia-acromesomelic-with-genital-anomalies" @default.
• MONDO_0012275 seeAlso "https://rarediseases.info.nih.gov/diseases/5447/fetal-valproate-syndrome" @default.
• MONDO_0012282 seeAlso "https://rarediseases.info.nih.gov/diseases/10054/al-gazali-syndrome" @default.
• MONDO_0012283 seeAlso "https://rarediseases.info.nih.gov/diseases/10063/cleft-palate-midfacial-hypoplasia-triangular-facies-and-sensorineural-hearing-loss" @default.
• MONDO_0012288 seeAlso "https://rarediseases.info.nih.gov/diseases/10058/iridogoniodysgenesis-and-skeletal-anomalies" @default.
• MONDO_0012291 seeAlso "https://rarediseases.info.nih.gov/diseases/10198/immunoglobulin-a-deficiency-2" @default.
• MONDO_0012296 seeAlso "https://rarediseases.info.nih.gov/diseases/10053/lipomyelomeningocele" @default.
• MONDO_0012308 seeAlso "https://rarediseases.info.nih.gov/diseases/10169/joubert-syndrome-with-renal-anomalies" @default.
• MONDO_0012316 seeAlso "https://rarediseases.info.nih.gov/diseases/10088/majeed-syndrome" @default.
• MONDO_0012323 seeAlso "https://rarediseases.info.nih.gov/diseases/9910/epidermolysis-bullosa-lethal-acantholytic" @default.
• MONDO_0012325 seeAlso "https://rarediseases.info.nih.gov/diseases/9754/nguyen-syndrome" @default.
• MONDO_0012345 seeAlso "https://rarediseases.info.nih.gov/diseases/12863/acral-peeling-skin-syndrome" @default.
• MONDO_0012348 seeAlso "https://rarediseases.info.nih.gov/diseases/10662/maturity-onset-diabetes-of-the-young-type-8" @default.
• MONDO_0012363 seeAlso "https://rarediseases.info.nih.gov/diseases/10395/retinitis-pigmentosa-32" @default.
• MONDO_0012367 seeAlso "https://rarediseases.info.nih.gov/diseases/10396/retinitis-pigmentosa-31" @default.
• MONDO_0012368 seeAlso "https://rarediseases.info.nih.gov/diseases/9741/aminoacylase-1-deficiency" @default.
• MONDO_0012371 seeAlso "https://rarediseases.info.nih.gov/diseases/9885/noonan-syndrome-3" @default.
• MONDO_0012373 seeAlso "https://rarediseases.info.nih.gov/diseases/9939/ectodermal-dysplasia-sensorineural-hearing-loss-and-distinctive-facial-features" @default.
• MONDO_0012374 seeAlso "https://rarediseases.info.nih.gov/diseases/9893/brachyphalangy-polydactyly-and-tibial-aplasiahypoplasia" @default.
• MONDO_0012382 seeAlso "https://rarediseases.info.nih.gov/diseases/9870/3-alpha-hydroxyacyl-coa-dehydrogenase-deficiency" @default.
• MONDO_0012385 seeAlso "https://rarediseases.info.nih.gov/diseases/9942/metaphyseal-chondrodysplasia-with-cone-shaped-epiphyses-normal-hair-and-normal-hands" @default.
• MONDO_0012386 seeAlso "https://rarediseases.info.nih.gov/diseases/9861/trichoscyphodysplasia" @default.
• MONDO_0012390 seeAlso "https://rarediseases.info.nih.gov/diseases/9946/arthrogryposis-multiplex-with-deafness-inguinal-hernias-and-early-death" @default.
• MONDO_0012391 seeAlso "https://rarediseases.info.nih.gov/diseases/2163/epilepsy-mental-deterioration-finnish-type" @default.
• MONDO_0012391 seeAlso "https://rarediseases.info.nih.gov/diseases/4010/northern-epilepsy" @default.
• MONDO_0012392 seeAlso "https://rarediseases.info.nih.gov/diseases/10322/2-methylbutyryl-coa-dehydrogenase-deficiency" @default.
• MONDO_0012394 seeAlso "https://rarediseases.info.nih.gov/diseases/9916/multiple-synostoses-syndrome-2" @default.
• MONDO_0012398 seeAlso "https://rarediseases.info.nih.gov/diseases/10648/retinal-cone-dystrophy-3a" @default.
• MONDO_0012414 seeAlso "https://rarediseases.info.nih.gov/diseases/1218/neuronal-ceroid-lipofuscinosis-10" @default.
• MONDO_0012416 seeAlso "https://rarediseases.info.nih.gov/diseases/10052/devriendt-syndrome" @default.
• MONDO_0012417 seeAlso "https://rarediseases.info.nih.gov/diseases/9846/heart-hand-syndrome-slovenian-type" @default.
• MONDO_0012423 seeAlso "https://rarediseases.info.nih.gov/diseases/10121/morm-syndrome" @default.
• MONDO_0012435 seeAlso "https://rarediseases.info.nih.gov/diseases/10344/3-methylglutaconic-aciduria-type-v" @default.
• MONDO_0012438 seeAlso "https://rarediseases.info.nih.gov/diseases/10709/pontocerebellar-hypoplasia-type-5" @default.
• MONDO_0012454 seeAlso "https://rarediseases.info.nih.gov/diseases/12634/acute-alcohol-sensitivity" @default.
• MONDO_0012455 seeAlso "https://rarediseases.info.nih.gov/diseases/8672/kleefstra-syndrome" @default.
• MONDO_0012463 seeAlso "https://rarediseases.info.nih.gov/diseases/10402/retinitis-pigmentosa-35" @default.
• MONDO_0012465 seeAlso "https://rarediseases.info.nih.gov/diseases/9965/hypercoagulability-syndrome-due-to-glycosylphosphatidylinositol-deficiency" @default.
• MONDO_0012468 seeAlso "https://rarediseases.info.nih.gov/diseases/9968/rhizomelic-dysplasia-scoliosis-and-retinitis-pigmentosa" @default.
• MONDO_0012473 seeAlso "https://rarediseases.info.nih.gov/diseases/10146/anomalous-origin-of-right-pulmonary-artery-familial" @default.

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