Nevroendokrine svulster

COL9A2 2218 NM_001852.4 1-32 ?Stickler syndrome, type V OMIM Epiphyseal dysplasia, multiple, 2 OMIM COL9A3 2219 NM_001853.3 1-32 Epiphyseal dysplasia, multiple, 3, with. or

immunohistochemical and molecular identity with gastrointestinal stromal tumor. Gastrointestinal stromal tumors: their origin and cause. Maeda H, Yamagata A, Nishikawa S, Yoshinaga

Antall pasienter behandlet for primær tumor (også primær metastatisk sykdom), alle tumorlokalisasjoner inkludert GIST (gastrointestinal stromal

FHL1 3702 NM_001449.4 99% Hemophagocytic lymphohistiocytosis, familial, 1 OMIM Emery-Dreifuss muscular dystrophy 6, X-linked OMIM Myopathy, X-linked, with postural muscle atrophy

FHL1 3702 NM_001449.4 99% Hemophagocytic lymphohistiocytosis, familial, 1 OMIM Emery-Dreifuss muscular dystrophy 6, X-linked OMIM Myopathy, X-linked, with postural muscle atrophy

FHL1 3702 NM_001449.4 99% Hemophagocytic lymphohistiocytosis, familial, 1 OMIM Emery-Dreifuss muscular dystrophy 6, X-linked OMIM Myopathy, X-linked, with postural muscle atrophy

FTL NM_000146.3 100% L-ferritin deficiency, dominant and recessive OMIM Neurodegeneration with brain iron accumulation 3 OMIM FTO NM_001080432.2 95% Growth retardation,

Pfeiffer syndrome OMIM Jackson-Weiss syndrome OMIM FGFR2 NM_000141.4 100% Crouzon syndrome OMIM. Saethre-Chotzen