Cluster(s) Orphanet Aandoening Orphacode Patiëntenorganisatie P PNR -U UNR Rare genetic diseases ABeta amyloidosis, Dutch type ORPHA:100006 Vereniging HCHWA-D P 14 U 2003 Rare neurological diseases Rare respiratory diseases Tubular duplication of the esophagus ORPHA:100048 Vereniging voor Ouderen en Kinderen met Slokdarmafsluiting (VOKS) P 124 U 495 Rare surgical thoracic diseases Rare surgical thoracic diseases Neurogenic thoracic outlet syndrome ORPHA:100073 RSI-vereniging P 305 U 6 Rare neurological diseases Neurogenic thoracic outlet syndrome ORPHA:100073 Spierziekten NL P 43 U 1418 Rare neoplastic diseases Laryngeal neuroendocrine tumor ORPHA:100083 ST NET-Groep P 62 U 1199 Rare odontological diseases Rare bone diseases Rare otorhinolaryngological diseases Rare skin diseases Rare surgical maxillo-facial diseases Rare neoplastic diseases Middle ear neuroendocrine tumor ORPHA:100084 ST NET-Groep P 62 U 1200 Rare odontological diseases Rare bone diseases Rare otorhinolaryngological diseases Rare skin diseases Rare surgical maxillo-facial diseases Rare endocrine diseases Thyroid tumor ORPHA:100087 Schildklier Organisatie NL (SON) P 60 U 1214 Rare neoplastic diseases Rare endocrine diseases Thyroid tumor ORPHA:100087 Schildklier Organisatie NL (SON) P 60 U 1213 Rare endocrine diseases Thyroid Tumor ORPHA:100087 Schildklier Organisatie NL (SON) P 60 U 1215 Rare neoplastic diseases Rare endocrine diseases Thyroid carcinoma ORPHA:100088 Schildklier Organisatie NL (SON) P 60 U 1216 Rare endocrine diseases Thyroid carcinoma ORPHA:100088 Schildklier Organisatie NL (SON) P 60 U 1219 Rare neoplastic diseases Rare endocrine diseases Thyroid carcinoma ORPHA:100088 Schildklier Organisatie NL (SON) P 60 U 1217 Rare neoplastic diseases Rare bone diseases Thyroid carcinoma ORPHA:100088 Schildklier Organisatie NL (SON) P 60 U 1218 Rare endocrine diseases Rare endocrine diseases Adrenal/paraganglial tumor ORPHA:100091 Bijniervereniging (NVACP) P 64 U 1141 Rare endocrine diseases Adrenal/paraganglial tumor ORPHA:100091 Bijniervereniging (NVACP) P 64 U 1142 Rare neoplastic diseases Rare urogenital diseases Rare endocrine diseases Adrenal/paraganglial tumor ORPHA:100091 Nlse Vereniging voor Patiënten met Paragangliomen (NVPG) P 29 U 1847 Rare neoplastic diseases Rare urogenital diseases Rare neoplastic diseases Gastroenteropancreatic neuroendocrine neoplasm ORPHA:100092 ST NET-Groep P 62 U 1201 Rare respiratory diseases Rare neoplastic diseases Thymic tumor ORPHA:100100 Longkankervereniging P 204 U 190 Rare respiratory diseases Rare neoplastic diseases Thymic tumor ORPHA:100100 Longkankervereniging P 204 U 191 Rare developmental anomalies during Rare non-syndromic intellectual disability ORPHA:101685 EMB NL P 285 U 67 embryogenesis Rare genetic diseases Rare non-syndromic intellectual disability ORPHA:101685 EMB NL P 285 U 68 Rare neurological diseases Rare developmental anomalies during Rare non-syndromic intellectual disability ORPHA:101685 ST Complex Care United P 306 U 3 embryogenesis Rare genetic diseases Rare non-syndromic intellectual disability ORPHA:101685 ST Complex Care United P 306 U 4 Rare neurological diseases Rare genetic diseases Rare non-syndromic intellectual disability ORPHA:101685 ST Grin Syndroom P 313 U 2004 Rare neurological diseases Rare cardiac diseases Genetic cardiac rhythm disease ORPHA:101934 Harteraad P 58 U 1238 Rare cardiac diseases Genetic cardiac rhythm disease ORPHA:101934 Harteraad P 58 U 1240 Rare circulatory system diseases Rare genetic diseases Rare cardiac diseases Genetic cardiac rhythm disease ORPHA:101934 Patiëntenvereniging Aangeboren Hartafwijkingen P 127 U 2019 Rare cardiac malformations Rare circulatory system diseases Rare genetic diseases Rare respiratory diseases Rare surgical thoracic diseases Rare systemic and rheumatological diseases Rare systemic or rheumatologic diseases of childhood Rare cardiac diseases Genetic cardiac rhythm disease ORPHA:101934 ST ICD dragers NL (STIN) P 206 U 181 Rare cardiac diseases Genetic cardiac rhythm disease ORPHA:101934 ST ICD dragers NL (STIN) P 206 U 183 Rare circulatory system diseases Rare genetic diseases Rare cardiac diseases Genetic cardiac rhythm disease ORPHA:101934 ST ICD dragers NL (STIN) P 206 U 182 Rare cardiac malformations Rare circulatory system diseases Rare genetic diseases Rare respiratory diseases Rare surgical thoracic diseases Rare systemic and rheumatological diseases Rare systemic or rheumatologic diseases of childhood Rare gastroenterologic diseases Rare pancreatic disease ORPHA:101937 Alvleeskliervereniging (AVKV) P 87 U 886 Rare gastroenterologic diseases Rare pancreatic disease ORPHA:101937 Alvleeskliervereniging (AVKV) P 87 U 887 Rare hepatic diseases Rare vascular liver disease ORPHA:101938 NLse Leverpatiënten Vereniging (NLV) P 19 U 1653 Rare hepatic diseases Rare hepatic and biliary tract tumor ORPHA:101943 NLse Leverpatiënten Vereniging (NLV) P 19 U 1655 Rare neoplastic diseases Rare gastroenterologic diseases Rare hepatic and biliary tract tumor ORPHA:101943 NLse Leverpatiënten Vereniging (NLV) P 19 U 1654 Rare neoplastic diseases Rare hepatic diseases Rare hepatic and biliary tract tumor ORPHA:101943 NLse Leverpatiënten Vereniging (NLV) P 19 U 1656 Rare allergic disease Rare pulmonary disease ORPHA:101944 Zonder patiëntenorganisatie P nvt U 520 Rare respiratory diseases Rare ophthalmic disorders Rare eye tumor ORPHA:101950 NFK-Patiëntenplatform zeldzame kankers P 18 U 1706 Rare bone diseases Rare Diabetes Mellitus ORPHA:101952 Diabetes Vereniging NL (DVN) P 103 U 667 Rare endocrine diseases Rare endocrine diseases Rare dyslipidemia ORPHA:101953 Harteraad P 58 U 1857 Rare inborn errors of metabolism Rare dyslipidemia ORPHA:101953 Harteraad P 58 U 1859 Rare endocrine diseases Rare dyslipidemia ORPHA:101953 Harteraad P 58 U 1858 Rare inborn errors of metabolism Rare endocrine diseases Rare dyslipidemia ORPHA:101953 Volwassenen, Kinderen en Stofwisselingsziekten (VKS) P 56 U 1294 Rare inborn errors of metabolism Rare dyslipidemia ORPHA:101953 Volwassenen, Kinderen en Stofwisselingsziekten (VKS) P 56 U 1296 Rare endocrine diseases Rare dyslipidemia ORPHA:101953 Volwassenen, Kinderen en Stofwisselingsziekten (VKS) P 56 U 1295 Rare inborn errors of metabolism Rare bone diseases Rare adrenal disease ORPHA:101954 Bijniervereniging (NVACP) P 64 U 1143 Rare endocrine diseases Rare endocrine diseases Rare adrenal disease ORPHA:101954 Bijniervereniging (NVACP) P 64 U 1145 Rare genetic diseases Rare ophthalmic disorders Rare endocrine diseases Rare adrenal disease ORPHA:101954 Bijniervereniging (NVACP) P 64 U 1144 Rare bone diseases Rare adrenal disease ORPHA:101954 Nlse Vereniging voor Patiënten met Paragangliomen (NVPG) P 29 U 2001 Rare endocrine diseases Rare endocrine diseases Rare adrenal disease ORPHA:101954 Nlse Vereniging voor Patiënten met Paragangliomen (NVPG) P 29 U 1848 Rare genetic diseases Rare ophthalmic disorders Rare endocrine diseases Rare adrenal disease ORPHA:101954 Nlse Vereniging voor Patiënten met Paragangliomen (NVPG) P 29 U 2000 Rare endocrine diseases Rare thyroid disease ORPHA:101955 Schildklier Organisatie NL (SON) P 60 U 1221 Rare genetic diseases Rare ophthalmic disorders Rare endocrine diseases Rare thyroid disease ORPHA:101955 Schildklier Organisatie NL (SON) P 60 U 1220 Rare bone diseases Polyendocrinopathy ORPHA:101956 Belangenvereniging Von Hippel-Lindau P 66 U 1120 Rare endocrine diseases Rare bone diseases Polyendocrinopathy ORPHA:101956 Nlse Vereniging voor Patiënten met Paragangliomen (NVPG) P 29 U 2002 Rare endocrine diseases Rare endocrine diseases Pituitary deficiency ORPHA:101957 NLse Hypofyse ST (NHS) P 65 U 1124 Rare endocrine diseases Pituitary deficiency ORPHA:101957 NLse Hypofyse ST (NHS) P 65 U 1125 Rare endocrine diseases Primary adrenal insufficiency ORPHA:101958 Bijniervereniging (NVACP) P 64 U 1146 Rare neoplastic diseases Rare urogenital diseases Rare immunological diseases Combined T and B cell immunodeficiency ORPHA:101972 ST voor Afweerstoornissen (SAS) P 72 U 1075 Rare genetic diseases Rare immunological diseases Immunodeficiency predominantly affecting antibody production ORPHA:101977 ST voor Afweerstoornissen (SAS) P 72 U 1076 Rare hematologic diseases Quantitative and/or qualitative congenital phagocyte defect ORPHA:101985 Shwachman Syndroom Support Holland (SSSH) P 76 U 1009 Rare immunological diseases Rare hematologic diseases Quantitative and/or qualitative congenital phagocyte defect ORPHA:101985 ST voor Afweerstoornissen (SAS) P 72 U 1077 Rare immunological diseases Rare hematologic diseases Constitutional neutropenia ORPHA:101987 ST Hematon P 81 U 956 Rare hematologic diseases Constitutional neutropenia ORPHA:101987 ST voor Afweerstoornissen (SAS) P 72 U 1977b Rare immunological diseases Immunodeficiency due to a complement cascade protein anomaly ORPHA:101992 ST voor Afweerstoornissen (SAS) P 72 U 1078 Rare systemic and rheumatological diseases Rare systemic or rheumatologic diseases of childhood Rare immunological diseases Periodic fever syndromes ORPHA:101995 ST KAISZ P 135 U 387 Rare systemic and rheumatological diseases Rare systemic or rheumatologic diseases of childhood Rare genetic diseases Rare immunological diseases Primary immunodeficiency ORPHA:101997 ST voor Afweerstoornissen (SAS) P 72 U 1083 Rare systemic and rheumatological diseases Rare systemic or rheumatologic diseases of childhood Rare immunological diseases Primary immunodeficiency ORPHA:101997 ST voor Afweerstoornissen (SAS) P 72 U 1081 Rare immunological diseases Primary immunodeficiency ORPHA:101997