Matches in Data.gov.be for { <http://data.gov.be/.well-known/genid/cfcba76b740b4245a85ec359572ede9e2-b2348> ?p ?o ?g. }
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Hyper-IgM syndrome with susceptibility to opportunistic infections" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Hypermobile Ehlers-Danlos syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Hypoparathyroidism-sensorineural deafness- renal disease syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Hypotonia-cystinuria syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "ICD10 A00–B99" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "ICD10 C00–D48" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "ICD10 D50–D89" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "ICD10 E00–E90" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "ICD10 F00–F99" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "ICD10 G00–G99" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "ICD10 H00–H59" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "ICD10 H60–H95" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "ICD10 I00–I99" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "ICD10 J00–J99" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "ICD10 K00–K93" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "ICD10 L00–L99" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "ICD10 M00–M99" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "ICD10 N00–N99" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "ICD10 O00–O99" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "ICD10 P00–P96" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "ICD10 Q00–Q96" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Immunodeficiency syndrome with autoimmunity" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Inclusion body myopathy with Paget disease of bone and frontotemporal dementia" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Infantile epilepsy syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Inherited Creutzfeldt-Jakob disease" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Inherited cancer-predisposing syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Intellectual disability-cardiac anomalies-short stature-joint laxity syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Intellectual disability-craniofacial dysmorphism- cryptorchidism syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Intellectual disability-developmental delay- contractures syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Intellectual disability-feeding difficulties- developmental delay-microcephaly syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Intellectual disability-microcephaly-strabismus- behavioral abnormalities syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Intellectual disability-severe speech delay-mild dysmorphism syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Intellectual disability-sparse hair-brachydactyly syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Interstitial lung disease due to SP-C deficiency" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Ischiovertebral syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Isolated Klippel-Feil syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Isolated Pierre Robin syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Isolated polycystic liver disease" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Jeune syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Joubert syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "KBG syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Kabuki syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Kagami-Ogata syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Kallmann syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Kearns-Sayre syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Keipert syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "King-Denborough syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Kleefstra syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Klinefelter syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Knobloch syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Koolen-De Vries syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Kostmann syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Kurzrippen-Polydaktylie-Syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Lamb-Shaffer syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Leber plus disease" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Legius syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Li-Fraumeni syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Linear nevus sebaceus syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Loeys-Dietz syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Lynch syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "MEND syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "MME-related autosomal dominant Charcot Marie Tooth disease type 2" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Macrocephaly-intellectual disability- neurodevelopmental disorder-small thorax syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Maffucci syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Malan overgrowth syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Mandibulofacial dysostosis-microcephaly syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Marfan syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Mayer-Rokitansky-Küster-Hauser syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "McCune-Albright syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Megalencephaly-capillary malformation- polymicrogyria syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Microcephaly-lymphedema-chorioretinopathy syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Microduplication Xp11.22p11.23 syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Moebius syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Monogenic disease with epilepsy" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Mowat-Wilson syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Muir-Torre syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Multifocal lymphangioendotheliomatosis- thrombocytopenia syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Multiple congenital anomalies-hypotonia- seizures syndrome type 2" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Musculocontractural Ehlers-Danlos syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Myasthenische Syndrome, kongenitale postsynaptische" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Myhre syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Myopathic Ehlers-Danlos syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "NARP syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "NLRC4-related familial cold autoinflammatory syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "NLRP12-associated hereditary periodic fever syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Nail-patella syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Nance-Horan syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "National institute for health and disability insurance (NIHDI)" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Niemann-Pick disease type B" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Niemann-Pick disease type C" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Noonan syndrome with multiple lentigines" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Noonan syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Noonan syndrome-like disorder with juvenile myelomonocytic leukemia" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Noonan syndrome-like disorder with loose anagen hair" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Occipital horn syndrome" @default.