48 träffar
ICD-10-SEICD-10-SE
G60.9 — Hereditär och idiopatisk neuropati, ospecificeradICD-10-SEICD-10-SE
G60.8 — Andra specificerade hereditära och idiopatiska neuropatierICD-10-SEICD-10-SE
G60.0 — Hereditär motorisk och sensorisk neuropatiICD-10-SEICD-10-SE
E80.0W — Annan och ospecificerad hereditär erytropoetisk porfyriICD-10-SEICD-10-SE
G11 — Hereditär ataxi (ärftlig koordinationsrubbning)ICD-10-SEICD-10-SE
N07 — Hereditär nefropati som ej klassificeras på annan platsICD-10-SEICD-10-SE
D56.4 — Hereditär persistens av fetalt hemoglobin [HPFH]ICD-10-SEICD-10-SE
D58.0 — Hereditär sfärocytosICD-10-SEICD-10-SE
D58.1 — Hereditär elliptocytosICD-10-SEICD-10-SE
D58.9 — Hereditär hemolytisk anemi, ospecificeradICD-10-SEICD-10-SE
D64.0 — Hereditär sideroblastisk anemiICD-10-SEICD-10-SE
D68.1 — Hereditär brist på faktor XIICD-10-SEICD-10-SE
D68.2 — Hereditär brist på andra koagulationsfaktorerICD-10-SEICD-10-SE
D72.1B — Eosinofili, hereditärICD-10-SEICD-10-SE
D80.0 — Hereditär hypogammaglobulinemiICD-10-SEICD-10-SE
D80.0A — Hereditär agammaglobulinemi, könsbundenICD-10-SEICD-10-SE
D80.0B — Hereditär agammaglobulinemi, autosomalt recessivICD-10-SEICD-10-SE
D80.0W — Annan hereditär hypogammaglobulinemiICD-10-SEICD-10-SE
E80.0 — Hereditär erytropoetisk porfyriICD-10-SEICD-10-SE
E80.2B — Hereditär koproporfyriICD-10-SEICD-10-SE
G11.4 — Hereditär spastisk paraparesICD-10-SEICD-10-SE
G11.9 — Hereditär ataxi, ospecificeradICD-10-SEICD-10-SE
G12.1 — Annan hereditär spinal muskelatrofiICD-10-SEICD-10-SE
G12.1A — Hereditär spinal muskelatrofi, seninfantil typ IIICD-10-SEICD-10-SE
G12.1B — Hereditär spinal muskelatrofi, juvenil typ IIIICD-10-SEICD-10-SE
G12.1W — Annan hereditär spinal muskelatrofiICD-10-SEICD-10-SE
G71.0A — Muskeldystrofi, hereditär, typ DuchenneICD-10-SEICD-10-SE
G71.0B — Muskeldystrofi, hereditär, typ Becker (benign)ICD-10-SEICD-10-SE
H31.2 — Hereditär korioidal dystrofiICD-10-SEICD-10-SE
H35.5 — Hereditär retinaldystrofiICD-10-SEICD-10-SE
I78.0 — Hereditär hemorragisk telangiektasiICD-10-SEICD-10-SE
G60.2 — Neuropati i samband med hereditär ataxiICD-10-SEICD-10-SE
D58.8 — Andra specificerade hereditära hemolytiska anemierICD-10-SEICD-10-SE
G11.8 — Andra specificerade hereditära ataxierICD-10-SEICD-10-SE
Q82.0 — Hereditärt lymfödemICD-10-SEICD-10-SE
L81.8G — Dyschromatosis symmetrica hereditaria [Dohi]ICD-10-SEICD-10-SE
G40.3D — Benigna neonatala kramper med eller utan hereditet