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ICD-10-CM×Ta bort filtret

17 träffar

ICD-10-CMICD-10-CM
G71.031 — Autosomal dominant limb girdle muscular dystrophy
ICD-10-CMICD-10-CM
E20.810 — Autosomal dominant hypocalcemia
ICD-10-CMICD-10-CM
G90.B — LMNB1-related autosomal dominant leukodystrophy
ICD-10-CMICD-10-CM
I67.850 — Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
ICD-10-CMICD-10-CM
E70.311 — Autosomal recessive ocular albinism
ICD-10-CMICD-10-CM
G71.032 — Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
ICD-10-CMICD-10-CM
Q95.2 — Balanced autosomal rearrangement in abnormal individual
ICD-10-CMICD-10-CM
Q95.3 — Balanced sex/autosomal rearrangement in abnormal individual
ICD-10-CMICD-10-CM
Q95.5 — Individual with autosomal fragile site
ICD-10-CMICD-10-CM
E83.822 — ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2
ICD-10-CMICD-10-CM
Q93.9 — Deletion from autosomes, unspecified
ICD-10-CMICD-10-CM
Q92.9 — Trisomy and partial trisomy of autosomes, unspecified
ICD-10-CMICD-10-CM
Q93 — Monosomies and deletions from the autosomes, not elsewhere classified
ICD-10-CMICD-10-CM
Q93.8 — Other deletions from the autosomes
ICD-10-CMICD-10-CM
Q93.89 — Other deletions from the autosomes
ICD-10-CMICD-10-CM
Q92 — Other trisomies and partial trisomies of the autosomes, not elsewhere classified
ICD-10-CMICD-10-CM
Q92.8 — Other specified trisomies and partial trisomies of autosomes
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