17 träffar
ICD-10-CMICD-10-CM
E70.311 — Autosomal recessive ocular albinismICD-10-CMICD-10-CM
E20.810 — Autosomal dominant hypocalcemiaICD-10-CMICD-10-CM
G71.031 — Autosomal dominant limb girdle muscular dystrophyICD-10-CMICD-10-CM
G90.B — LMNB1-related autosomal dominant leukodystrophyICD-10-CMICD-10-CM
Q95.2 — Balanced autosomal rearrangement in abnormal individualICD-10-CMICD-10-CM
Q95.3 — Balanced sex/autosomal rearrangement in abnormal individualICD-10-CMICD-10-CM
Q95.5 — Individual with autosomal fragile siteICD-10-CMICD-10-CM
Q93.9 — Deletion from autosomes, unspecifiedICD-10-CMICD-10-CM
Q92.9 — Trisomy and partial trisomy of autosomes, unspecifiedICD-10-CMICD-10-CM
Q93.8 — Other deletions from the autosomesICD-10-CMICD-10-CM
Q93.89 — Other deletions from the autosomesICD-10-CMICD-10-CM
Q92.8 — Other specified trisomies and partial trisomies of autosomes