Matches in Data.gov.be for { <http://data.gov.be/.well-known/genid/cfcba76b740b4245a85ec359572ede9e2-b2348> ?p ?o ?g. }
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Oculocerebrofacial syndrome- Kaufman type" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Oculocerebrorenal syndrome of Lowe" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Oculofaciocardiodental syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Ollier disease" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Omenn syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Ondine syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Optic atrophy-peripheral neuropathy- developmental delay syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Orofaciodigital syndrome type 1" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Otomandibular syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Overgrowth syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "PEHO syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "PENS syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "PHACE syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "PIK3CA-related overgrowth syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "PTEN hamartoma tumor syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "PURA-related severe neonatal hypotonia- seizures-encephalopathy syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Peeling skin syndrome type acral" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Pelizaeus-Merzbacher disease" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Pendred syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Peroxisomal disease" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Persistent Müllerian duct syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Peters plus syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Peutz-Jeghers syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Pfeiffer syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Pitt-Hopkins syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Pitt-Hopkins-like syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Pituitary stalk interruption syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Poland syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Polyvalvular heart disease syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Prader-Willi syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Primary Fanconi syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Primary tethered cord syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Proteus syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Proximal 16p11.2 microdeletion syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Proximal 16p11.2 microduplication syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Rare bone disease" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Rare cardiac disease" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Rare disease with autism" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Rare disease with malignant hyperthermia" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Rare endocrine disease" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Rare endocrine growth disease" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Rare gastroenterologic disease" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Rare genetic disease" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Rare genetic hepatic disease" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Rare neurodegenerative disease" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Rare neurologic disease with psychiatric involvement" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Rare neurologic disease" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Rare renal disease" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Renal cysts and diabetes syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Rett syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Ring chromosome 18 syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Ring chromosome 20 syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Ring chromosome 22 syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Roberts syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Rothmund-Thomson syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Rubinstein-Taybi syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "SIN3A-related intellectual disability syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Saethre-Chotzen syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Senior-Boichis syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Senior-Loken syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Sensory ataxic neuropathy-dysarthria- ophthalmoparesis syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Severe feeding difficulties-failure to thrive- microcephaly due to ASXL3 deficiency syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Severe intellectual disability-poor language- strabismus-grimacing face-long fingers syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Severe intellectual disability-progressive spastic diplegia syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Short rib-polydactyly syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Short stature-advanced bone age-early-onset osteoarthritis syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Short stature-optic atrophy-Pelger-Huët anomaly syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Silver-Russell syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Simpson-Golabi-Behmel syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Smith-Lemli-Opitz syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Smith-Magenis syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Sotos syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Sporadic idiopathic steroid-resistant nephrotic syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Stargardt disease" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Stickler syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Sturge-Weber syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Stüve-Wiedemann syndrome" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Symptomatic form of fragile X syndrome in female carrier" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Syndrome 3M" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Syndrome 47,XYY" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Syndrome ADNP" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Syndrome BOR" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Syndrome CHARGE" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Syndrome CLOVES" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Syndrome HANAC" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Syndrome KBG" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Syndrome Kabuki" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Syndrome MEND" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Syndrome NARP" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Syndrome Noonan-like avec cheveux anagènes caducs" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Syndrome Noonan-like avec leucémie myélomonocytaire juvénile" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Syndrome PEHO" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Syndrome PHACE" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Syndrome TARP" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Syndrome WAGR" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Syndrome acro-réno-oculaire" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Syndrome angio-ostéo-hypertrophique" @default.
- cfcba76b740b4245a85ec359572ede9e2-b2348 keyword "Syndrome associated with hypertrophic cardiomyopathy" @default.