FRINK Linked Data Fragments server

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

• MONDO_0007215 seeAlso "https://rarediseases.info.nih.gov/diseases/978/brachydactyly-type-a1" @default.
• MONDO_0007216 seeAlso "https://rarediseases.info.nih.gov/diseases/979/brachydactyly-type-a2" @default.
• MONDO_0007216 seeAlso "https://rarediseases.info.nih.gov/diseases/989/brachymesophalangy-type-2" @default.
• MONDO_0007217 seeAlso "https://rarediseases.info.nih.gov/diseases/963/brachydactyly-type-a3" @default.
• MONDO_0007218 seeAlso "https://rarediseases.info.nih.gov/diseases/990/brachydactyly-type-a4" @default.
• MONDO_0007219 seeAlso "https://rarediseases.info.nih.gov/diseases/983/brachydactyly-type-a6" @default.
• MONDO_0007226 seeAlso "https://rarediseases.info.nih.gov/diseases/881/biemond-syndrome-type-1" @default.
• MONDO_0007235 seeAlso "https://rarediseases.info.nih.gov/diseases/3212/branchiooculofacial-syndrome" @default.
• MONDO_0007238 seeAlso "https://rarediseases.info.nih.gov/diseases/9489/absent-breasts-and-nipples" @default.
• MONDO_0007245 seeAlso "https://rarediseases.info.nih.gov/diseases/3967/autosomal-dominant-cafe-au-lait-spots" @default.
• MONDO_0007247 seeAlso "https://rarediseases.info.nih.gov/diseases/9598/idiopathic-basal-ganglia-calcification-childhood-onset" @default.
• MONDO_0007249 seeAlso "https://rarediseases.info.nih.gov/diseases/1062/camptobrachydactyly" @default.
• MONDO_0007250 seeAlso "https://rarediseases.info.nih.gov/diseases/9448/familial-streblodactyly" @default.
• MONDO_0007252 seeAlso "https://rarediseases.info.nih.gov/diseases/2553/gordon-syndrome" @default.
• MONDO_0007269 seeAlso "https://rarediseases.info.nih.gov/diseases/1104/cardiomyopathy-dilated-with-conduction-defect-type-1" @default.
• MONDO_0007271 seeAlso "https://rarediseases.info.nih.gov/diseases/9799/familial-cutaneous-collagenoma" @default.
• MONDO_0007273 seeAlso "https://rarediseases.info.nih.gov/diseases/10546/paragangliomas-4" @default.
• MONDO_0007276 seeAlso "https://rarediseases.info.nih.gov/diseases/26/cat-eye-syndrome" @default.
• MONDO_0007295 seeAlso "https://epilepsydiagnosis.org/syndrome/ects-overview.html" @default.
• MONDO_0007295 seeAlso "https://rarediseases.info.nih.gov/diseases/10287/benign-rolandic-epilepsy-bre" @default.
• MONDO_0007300 seeAlso "https://rarediseases.info.nih.gov/diseases/10073/cerebral-sarcoma" @default.
• MONDO_0007308 seeAlso "https://rarediseases.info.nih.gov/diseases/1248/charcot-marie-tooth-disease-type-2a" @default.
• MONDO_0007309 seeAlso "https://rarediseases.info.nih.gov/diseases/1245/charcot-marie-tooth-disease-type-1a" @default.
• MONDO_0007313 seeAlso "https://rarediseases.info.nih.gov/diseases/412/cheilitis-glandularis" @default.
• MONDO_0007315 seeAlso "https://rarediseases.info.nih.gov/diseases/6036/cherubism" @default.
• MONDO_0007320 seeAlso "https://rarediseases.info.nih.gov/diseases/10139/chondrocalcinosis-due-to-apatite-crystal-deposition" @default.
• MONDO_0007321 seeAlso "https://rarediseases.info.nih.gov/diseases/1298/chondrodysplasia-punctata-sheffield-type" @default.
• MONDO_0007336 seeAlso "https://rarediseases.info.nih.gov/diseases/1896/dominant-cleft-palate" @default.
• MONDO_0007337 seeAlso "https://rarediseases.info.nih.gov/diseases/1391/cleft-palate-lateral-synechia-syndrome" @default.
• MONDO_0007339 seeAlso "https://rarediseases.info.nih.gov/diseases/2071/ectropion-inferior-cleft-lip-and-or-palate" @default.
• MONDO_0007341 seeAlso "https://rarediseases.info.nih.gov/diseases/5532/cleidorhizomelic-syndrome" @default.
• MONDO_0007346 seeAlso "https://rarediseases.info.nih.gov/diseases/9418/cochleosaccular-degeneration-of-the-inner-ear-and-progressive-cataracts" @default.
• MONDO_0007352 seeAlso "https://rarediseases.info.nih.gov/diseases/4106/renal-coloboma-syndrome" @default.
• MONDO_0007368 seeAlso "https://rarediseases.info.nih.gov/diseases/1522/copper-deficiency-familial-benign" @default.
• MONDO_0007369 seeAlso "https://rarediseases.info.nih.gov/diseases/6619/hereditary-coproporphyria" @default.
• MONDO_0007379 seeAlso "https://rarediseases.info.nih.gov/diseases/9688/meesmann-corneal-dystrophy" @default.
• MONDO_0007388 seeAlso "https://rarediseases.info.nih.gov/diseases/1551/costocoracoid-ligament-congenitally-short" @default.
• MONDO_0007392 seeAlso "https://rarediseases.info.nih.gov/diseases/1558/coxoauricular-syndrome" @default.
• MONDO_0007395 seeAlso "https://rarediseases.info.nih.gov/diseases/1571/craniofacial-deafness-hand-syndrome" @default.
• MONDO_0007400 seeAlso "https://rarediseases.info.nih.gov/diseases/6796/jackson-weiss-syndrome" @default.
• MONDO_0007401 seeAlso "https://rarediseases.info.nih.gov/diseases/1592/dandy-walker-malformation-with-sagittal-craniosynostosis-and-hydrocephalus" @default.
• MONDO_0007405 seeAlso "https://rarediseases.info.nih.gov/diseases/6206/crouzon-syndrome" @default.
• MONDO_0007412 seeAlso "https://rarediseases.info.nih.gov/diseases/332/beare-stevenson-cutis-gyrata-syndrome" @default.
• MONDO_0007413 seeAlso "https://rarediseases.info.nih.gov/diseases/9487/cyprus-facial-neuromusculoskeletal-syndrome" @default.
• MONDO_0007415 seeAlso "https://rarediseases.info.nih.gov/diseases/8295/mitochondrial-complex-iii-deficiency" @default.
• MONDO_0007420 seeAlso "https://rarediseases.info.nih.gov/diseases/4732/autosomal-dominant-deafness-onychodystrophy-syndrome" @default.
• MONDO_0007428 seeAlso "https://rarediseases.info.nih.gov/diseases/1686/deafness-craniofacial-syndrome" @default.
• MONDO_0007435 seeAlso "https://rarediseases.info.nih.gov/diseases/5643/dentatorubral-pallidoluysian-atrophy" @default.
• MONDO_0007436 seeAlso "https://rarediseases.info.nih.gov/diseases/1807/dentin-dysplasia-type-1" @default.
• MONDO_0007442 seeAlso "https://rarediseases.info.nih.gov/diseases/10144/dentinogenesis-imperfecta-type-3" @default.
• MONDO_0007445 seeAlso "https://rarediseases.info.nih.gov/diseases/8550/dermatopathia-pigmentosa-reticularis" @default.
• MONDO_0007448 seeAlso "https://rarediseases.info.nih.gov/diseases/9480/familial-dermographism" @default.
• MONDO_0007452 seeAlso "https://rarediseases.info.nih.gov/diseases/3418/maturity-onset-diabetes-of-the-young-type-1" @default.
• MONDO_0007453 seeAlso "https://rarediseases.info.nih.gov/diseases/10657/maturity-onset-diabetes-of-the-young-type-2" @default.
• MONDO_0007469 seeAlso "https://rarediseases.info.nih.gov/diseases/9672/double-nails-on-the-fifth-toe" @default.
• MONDO_0007471 seeAlso "https://rarediseases.info.nih.gov/diseases/1912/doyne-honeycomb-retinal-dystrophy" @default.
• MONDO_0007473 seeAlso "https://rarediseases.info.nih.gov/diseases/6288/duane-syndrome" @default.
• MONDO_0007474 seeAlso "https://rarediseases.info.nih.gov/diseases/9743/duodenal-ulcer-due-to-antral-g-cell-hyperfunction" @default.
• MONDO_0007478 seeAlso "https://rarediseases.info.nih.gov/diseases/83/kenny-caffey-syndrome-type-2" @default.
• MONDO_0007479 seeAlso "https://rarediseases.info.nih.gov/diseases/6294/dwarfism-levi-type" @default.
• MONDO_0007481 seeAlso "https://rarediseases.info.nih.gov/diseases/3224/leri-weill-dyschondrosteosis" @default.
• MONDO_0007482 seeAlso "https://rarediseases.info.nih.gov/diseases/1994/dyschondrosteosis-nephritis" @default.
• MONDO_0007485 seeAlso "https://rarediseases.info.nih.gov/diseases/6299/dyskeratosis-congenita-autosomal-dominant" @default.
• MONDO_0007489 seeAlso "https://rarediseases.info.nih.gov/diseases/2019/dysplasia-epiphysealis-hemimelica" @default.
• MONDO_0007490 seeAlso "https://rarediseases.info.nih.gov/diseases/1128/carpotarsal-osteochondromatosis" @default.
• MONDO_0007491 seeAlso "https://rarediseases.info.nih.gov/diseases/10059/dystelephalangy" @default.
• MONDO_0007492 seeAlso "https://rarediseases.info.nih.gov/diseases/2027/early-onset-generalized-dystonia" @default.
• MONDO_0007507 seeAlso "https://rarediseases.info.nih.gov/diseases/2336/absence-of-fingerprints-congenital-milia" @default.
• MONDO_0007508 seeAlso "https://rarediseases.info.nih.gov/diseases/5690/rapp-hodgkin-syndrome" @default.
• MONDO_0007511 seeAlso "https://rarediseases.info.nih.gov/diseases/2055/ectodermal-dysplasia-trichoodontoonychial-type" @default.
• MONDO_0007519 seeAlso "https://rarediseases.info.nih.gov/diseases/2074/edinburgh-malformation-syndrome" @default.
• MONDO_0007525 seeAlso "https://rarediseases.info.nih.gov/diseases/2084/arthrochalasia-ehlers-danlos-syndrome" @default.
• MONDO_0007529 seeAlso "https://rarediseases.info.nih.gov/diseases/10103/elastosis-perforans-serpiginosa" @default.
• MONDO_0007534 seeAlso "https://rarediseases.info.nih.gov/diseases/3343/beckwith-wiedemann-syndrome" @default.
• MONDO_0007539 seeAlso "https://rarediseases.info.nih.gov/diseases/2117/encephalopathy-recurrent-of-childhood" @default.
• MONDO_0007540 seeAlso "https://rarediseases.info.nih.gov/diseases/3829/multiple-endocrine-neoplasia-type-1" @default.
• MONDO_0007544 seeAlso "https://rarediseases.info.nih.gov/diseases/10521/familial-eosinophilia" @default.
• MONDO_0007548 seeAlso "https://rarediseases.info.nih.gov/diseases/10010/transient-bullous-dermolysis-of-the-newborn" @default.
• MONDO_0007550 seeAlso "https://rarediseases.info.nih.gov/diseases/2141/epidermolysis-bullosa-simplex-dowling-meara-type" @default.
• MONDO_0007551 seeAlso "https://rarediseases.info.nih.gov/diseases/2146/epidermolysis-bullosa-simplex-localized" @default.
• MONDO_0007555 seeAlso "https://rarediseases.info.nih.gov/diseases/2148/epidermolysis-bullosa-simplex-ogna-type" @default.
• MONDO_0007556 seeAlso "https://rarediseases.info.nih.gov/diseases/9737/epidermolysis-bullosa-simplex-with-mottled-pigmentation" @default.
• MONDO_0007558 seeAlso "https://rarediseases.info.nih.gov/diseases/2170/epilepsy-benign-occipital" @default.
• MONDO_0007561 seeAlso "https://rarediseases.info.nih.gov/diseases/2180/multiple-epiphyseal-dysplasia-1" @default.
• MONDO_0007564 seeAlso "https://rarediseases.info.nih.gov/diseases/9452/pilomatrixoma" @default.
• MONDO_0007566 seeAlso "https://rarediseases.info.nih.gov/diseases/3090/multiple-self-healing-squamous-epithelioma" @default.
• MONDO_0007568 seeAlso "https://rarediseases.info.nih.gov/diseases/9876/aortic-aneurysm-familial-thoracic-4" @default.
• MONDO_0007569 seeAlso "https://rarediseases.info.nih.gov/diseases/9259/familial-erythema-nodosum" @default.
• MONDO_0007572 seeAlso "https://rarediseases.info.nih.gov/diseases/9843/familial-erythrocytosis-1" @default.
• MONDO_0007585 seeAlso "https://rarediseases.info.nih.gov/diseases/2204/exostoses-multiple-type-1" @default.
• MONDO_0007586 seeAlso "https://rarediseases.info.nih.gov/diseases/2205/exostoses-multiple-type-2" @default.
• MONDO_0007600 seeAlso "https://rarediseases.info.nih.gov/diseases/9118/primary-fanconi-syndrome" @default.
• MONDO_0007603 seeAlso "https://rarediseases.info.nih.gov/diseases/8234/feltys-syndrome" @default.
• MONDO_0007604 seeAlso "https://rarediseases.info.nih.gov/diseases/61/femoral-facial-syndrome" @default.
• MONDO_0007609 seeAlso "https://rarediseases.info.nih.gov/diseases/6509/gingival-fibromatosis-1" @default.
• MONDO_0007610 seeAlso "https://rarediseases.info.nih.gov/diseases/2324/gingival-fibromatosis-with-hypertrichosis" @default.
• MONDO_0007615 seeAlso "https://rarediseases.info.nih.gov/diseases/155/laurin-sandrow-syndrome" @default.
• MONDO_0007617 seeAlso "https://rarediseases.info.nih.gov/diseases/9945/hypertrichosis-hyperkeratosis-mental-retardation-and-distinctive-facial-features" @default.
• MONDO_0007620 seeAlso "https://rarediseases.info.nih.gov/diseases/6450/fish-eye-disease" @default.
• MONDO_0007621 seeAlso "https://rarediseases.info.nih.gov/diseases/6455/floating-harbor-syndrome" @default.

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