ICD-11-MMS
ICD-11-MMS ICD11分類(ICD-11-MMS) > CHAPTER20 発生異常(Developmental anomalies) > BlockL1-LD2 多発性の発生異常又は発生異常症候群(Multiple developmental anomalies or syndromes) > LD2H 症候群性遺伝性難聴(Syndromic genetic deafness) > LD2H.Y その他の明示された症候群性遺伝性難聴(Other specified syndromic genetic deafness)
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LD2H.Y その他の明示された症候群性遺伝性難聴(Other specified syndromic genetic deafness)
分類ID 分類名 ICD11
1 10224290 その他の明示された症候群性遺伝性難聴(Other specified syndromic genetic deafness) LD2H.Y
2 20071316 白皮症・黒色鬢毛・腸神経細胞遊走障害・感音性難聴(Albinism - black lock - cell migration disorder of the neurocytes of the gut - sensorineural deafness) LD2H.Y
3 20071317 ABCD[白皮症・黒色鬢毛・腸神経細胞遊走障害・感音性難聴]症候群(ABCD - [Albinism - black lock - cell migration disorder of the neurocytes of the gut - sensorineural deafness] syndrome) LD2H.Y
4 20071318 白皮症・難聴症候群(Albinism-deafness syndrome) LD2H.Y
5 20071319 アルストラム症候群(Alström syndrome) LD2H.Y
6 20071320 運動失調・難聴・知的障害症候群(Ataxia - deafness - intellectual disability syndrome) LD2H.Y
7 20071321 アサバスカン脳幹異発生症候群(Athabaskan brainstem dysgenesis syndrome) LD2H.Y
8 20071322 粥状硬化症・難聴・糖尿病・てんかん・腎症(Atherosclerosis - deafness - diabetes - epilepsy - nephropathy) LD2H.Y
9 20071323 両側性小耳・難聴・口蓋裂(Bilateral microtia - deafness - cleft palate) LD2H.Y
10 20071324 ボスレイ・サリー・アロレイニー症候群(Bosley-Salih-Alorainy syndrome) LD2H.Y
11 20071325 ブラウン・ヴァイアレット・ヴァンレアル症候群(Brown-Vialetto-van Laere syndrome) LD2H.Y
12 20071326 感音性難聴・橋球麻痺(Sensorineural hearing loss - pontobulbar palsy) LD2H.Y
13 20071327 白内障・運動失調・難聴(Cataract - ataxia - deafness) LD2H.Y
14 20071328 白内障・難聴・性腺機能低下症(Cataract - deafness - hypogonadism) LD2H.Y
15 20071329 尾肢・難聴(Caudal appendage - deafness) LD2H.Y
16 20071330 中枢神経系石灰化・難聴・尿細管性アシドーシス・貧血(Central nervous system calcification - deafness - tubular acidosis - anaemia) LD2H.Y
17 20071331 後鼻孔閉鎖・難聴・心疾患・形態異常(Choanal atresia - deafness - cardiac defects - dysmorphism) LD2H.Y
18 20071332 コロイデレミア・難聴・肥満症(Choroideremia - deafness - obesity) LD2H.Y
19 20071333 口唇裂又は口蓋裂・難聴・仙椎脂肪腫(Cleft lip or palate - deafness - sacral lipoma) LD2H.Y
20 20071334 蝸牛球形嚢変性・白内障(Cochleosaccular degeneration - cataract) LD2H.Y
21 20071335 角膜知覚麻痺・難聴・知的障害(Corneal anaesthesia - deafness - intellectual disability) LD2H.Y
22 20071336 角膜ジストロフィー・感音性難聴(Corneal dystrophy - perceptive deafness) LD2H.Y
23 20071337 頭蓋顔面・難聴・手症候群(Craniofacial-deafness-hand syndrome) LD2H.Y
24 20071338 難聴・視覚障害・低色素症候群、イエメン型(Deaf blind hypopigmentation syndrome, Yemenite type) LD2H.Y
25 20071339 難聴・頭蓋顔面症候群(Deafness - craniofacial syndrome) LD2H.Y
26 20071340 難聴・骨端異形成・低身長症(Deafness - epiphyseal dysplasia - short stature) LD2H.Y
27 20071341 難聴・生殖器異常・中手骨及び中足骨癒合症(Deafness - genital anomalies - metacarpal and metatarsal synostosis) LD2H.Y
28 20071342 難聴・性腺機能低下症(Deafness - hypogonadism) LD2H.Y
29 20071343 難聴・知的障害、マーチン・プロブスト型(Deafness - intellectual deficit syndrome, Martin-Probst type) LD2H.Y
30 20071344 マーティン・プロブスト症候群(Martin-Probst syndrome) LD2H.Y
31 20071345 難聴・乏歯症(Deafness - oligodontia) LD2H.Y
32 20071346 難聴・末梢神経障害・動脈疾患(Deafness - peripheral neuropathy - arterial disease) LD2H.Y
33 20071347 難聴・骨異形成・口唇肉芽腫(Deafness - skeletal dysplasia - lip granuloma) LD2H.Y
34 20071348 ファウンテン症候群(Fountain syndrome) LD2H.Y
35 20071349 難聴・小腸憩室症・ニューロパチー(Deafness - small bowel diverticulosis - neuropathy) LD2H.Y
36 20071350 難聴・白斑・アカラシア(Deafness - vitiligo - achalasia) LD2H.Y
37 20071351 難聴・不妊症候群(Deafness-infertility syndrome) LD2H.Y
38 20071352 15q15.3欠失症候群(15q15.3 deletion syndrome) LD2H.Y
39 20071353 モノソミー15q15.3(Monosomy 15q15.3) LD2H.Y
40 20071354 15q15.3欠失(15q15.3 deletion) LD2H.Y
41 20071355 象牙質形成不全・低身長症・難聴・知的障害(Dentinogenesis imperfecta - short stature - hearing loss - intellectual deficit) LD2H.Y
42 20071356 発育遅延・難聴、ヒルデブラント型(Developmental delay - deafness, Hildebrand type) LD2H.Y
43 20071357 発生形態異常・難聴・ジストニア(Developmental malformations - deafness - dystonia) LD2H.Y
44 20071358 アーミン表現型(Ermine phenotype) LD2H.Y
45 20071359 歯肉線維腫症・進行性難聴(Gingival fibromatosis - progressive deafness) LD2H.Y
46 20071360 聴覚障害・家族性唾液腺アルドステロン不応症(Hearing loss - familial salivary gland insensitivity to aldosterone) LD2H.Y
47 20071361 ヒルシュスプルング病・難聴・多指趾症(Hirschsprung disease - deafness - polydactyly) LD2H.Y
48 20071362 尿道下裂・眼間開離・コロボーマ及び難聴(Hypospadias-hypertelorism-coloboma and deafness) LD2H.Y
49 20071363 虹彩異形成・眼間開離・難聴(Iris dysplasia - hypertelorism - deafness) LD2H.Y
50 20071364 難聴及び視神経萎縮症を伴う重症運動失調症(Lethal ataxia with deafness and optic atrophy) LD2H.Y
51 20071365 アーツ症候群(Arts syndrome) LD2H.Y
52 20071366 リポジストロフィー・知的障害・難聴(Lipodystrophy - intellectual deficit - deafness) LD2H.Y
53 20071367 ロウ・コーン・コーエン症候群(Lowe-Kohn-Cohen syndrome) LD2H.Y
54 20071368 難聴・腎炎・直腸肛門形態異常(Deafness - nephritis - anorectal malformation) LD2H.Y
55 20071369 ミトコンドリア糖尿病及び難聴(Maternally inherited diabetes and deafness) LD2H.Y
56 20071370 ミトコンドリア糖尿病(Mitochondrial diabetes) LD2H.Y
57 20071371 上顎鼻異形成(Maxillonasal dysplasia) LD2H.Y
58 20071372 知的障害・腸症・難聴・ニューロパチー・魚鱗癬・皮膚角化症候群(Intellectual disability – enteropathy – deafness – neuropathy – ichthyosis – keratoderma syndrome) LD2H.Y
59 20071373 知的障害・腸症・難聴・ニューロパチー・魚鱗癬・皮膚角化症候群(Mental retardation – enteropathy – deafness – neuropathy – ichthyosis – keratoderma syndrome) LD2H.Y
60 20071374 MEDNIK[知的障害・腸症・難聴・ニューロパチー・魚鱗癬・皮膚角化]症候群(MEDNIK - [Mental retardation – enteropathy – deafness – neuropathy – ichthyosis – keratoderma] syndrome) LD2H.Y
61 20071375 小頭・難聴・知的障害(Microcephaly - deafness - intellectual disability) LD2H.Y
62 20071376 矮小歯・小耳症1型・難聴(Microdontia - microtia type I - deafness) LD2H.Y
63 20071377 迷路低形成を伴う難聴・小耳症、及び矮小歯(Deafness with labyrinthine aplasia, microtia, and microdontia) LD2H.Y
64 20071378 僧帽弁閉鎖不全・難聴・骨格異常(Mitral regurgitation - deafness - skeletal anomalies) LD2H.Y
65 20071379 ミオクローヌス・小脳性運動失調・難聴(Myoclonus - cerebellar ataxia - deafness) LD2H.Y
66 20071380 N症候群(N syndrome) LD2H.Y
67 20071381 腎症・難聴・副甲状腺機能亢進症(Nephropathy - deafness - hyperparathyroidism) LD2H.Y
68 20071382 ネフローゼ・難聴・尿路・指趾形態異常(Nephrosis - deafness - urinary tract - digital malformations) LD2H.Y
69 20071383 好中球減少症・単球減少症・難聴(Neutropaenia - monocytopaenia - deafness) LD2H.Y
70 20071384 オリーブ橋小脳萎縮症・難聴(Olivopontocerebellar atrophy - deafness) LD2H.Y
71 20071385 骨軟骨異形成性低身長症・難聴・網膜色素変性症(Osteochondrodysplatic nanism - deafness - retinitis pigmentosa) LD2H.Y
72 20071386 末梢神経障害、フィスカーストランド型(Peripheral neuropathy, Fiskerstrand type) LD2H.Y
73 20071387 ペロー症候群(Perrault syndrome) LD2H.Y
74 20071388 フォコメリア・指趾欠損・難聴・洞性不整脈(Phocomelia - ectrodactyly - deafness - sinus arrhythmia) LD2H.Y
75 20071389 カーンズ・セイヤー症候群による肥大型心筋症(Hypertrophic cardiomyopathy due to Kearns–Sayre syndrome) LD2H.Y
76 20071390 進行性感音性難聴・肥大型心筋症(progressive sensorineural hearing loss - hypertrophic cardiomyopathy) LD2H.Y
77 20071391 進行性感音性難聴を伴う肥大型心筋症(Hypertrophic cardiomyopathy associated with progressive sensorineural hearing loss) LD2H.Y
78 20071392 網膜色素変性・知的障害・難聴・性器低形成(Retinitis pigmentosa - intellectual disability - deafness - hypogenitalism) LD2H.Y
79 20071393 リチャーズ・ランドル症候群(Richards-Rundle syndrome) LD2H.Y
80 20071394 統合失調症・知的障害・難聴・網膜炎(Schizophrenia - intellectual disability - deafness - retinitis) LD2H.Y
81 20071395 感音性難聴・早発白髪・本態性振戦(Sensorineural hearing loss - early greying - essential tremor) LD2H.Y
82 20071396 SeSAME症候群(SeSAME syndrome) LD2H.Y
83 20071397 EAST症候群(EAST syndrome) LD2H.Y
84 20071398 低身長症・難聴・好中球機能不全・形態異常(Short stature - deafness - neutrophil dysfunction - dysmorphism) LD2H.Y
85 20071399 痙性対麻痺・難聴(Spastic paraparesis - deafness) LD2H.Y
86 20071400 裂手・裂足・難聴(Split hand - split foot - deafness) LD2H.Y
87 20071401 耳垂肥厚・伝音性難聴(Thickened earlobes - conductive deafness) LD2H.Y
88 20071402 難聴・視神経萎縮症候群(Deafness - optic atrophy syndrome) LD2H.Y
89 20071403 視神経萎縮・難聴・眼筋麻痺・ミオパチー(Optic atrophy, deafness, ophthalmoplegia, myopathy) LD2H.Y
90 20071404 常染色体顕性視神経萎縮症及び先天性難聴(Autosomal dominant optic atrophy and congenital deafness) LD2H.Y
91 20071405 眼型白皮症・遅発性感音難聴(Ocular albinism - late-onset sensorineural deafness) LD2H.Y
92 20071406 痙性対麻痺・腎炎・難聴(Spastic paraplegia - nephritis - deafness) LD2H.Y
93 20071407 骨幹端異形成症・知的障害・伝音性難聴(Metaphyseal dysostosis - intellectual deficit - conductive deafness) LD2H.Y
94 20071408 ナックルパッド・爪甲白斑症・感音性難聴(Knuckle pads – leukonychia – sensorineural deafness) LD2H.Y
95 20071409 バート・パンフリー症候群(Bart-Pumphrey syndrome (MIM 149200)) LD2H.Y
96 20071410 アルポート症候群(Alport syndrome) LD2H.Y
97 20071411 アルポート症候群、常染色体顕性(Alport syndrome, autosomal dominant) LD2H.Y
98 20071412 アルポート症候群、常染色体潜性(Alport syndrome, autosomal recessive) LD2H.Y
99 20071413 アルポート症候群、X連鎖性(Alport syndrome, X-linked) LD2H.Y
100 20071414 アルポート症候群、X連鎖性びまん性平滑筋腫(Alport syndrome, X-linked diffuse leiomyomatosis) LD2H.Y
101 20071415 心臓聴覚症候群(Cardioauditory syndrome) LD2H.Y