UR-DBMS-検索結果一覧

UR-DBMS-検索結果一覧



疾患No
英語疾患名
日本語疾患名
症状
コメント
文献
検索方法 すべての条件が一致

前ページ 検索結果 9840件中3726-3750件目 次ページ



項番 疾患No 英語疾患名
3726 601869 Deafness, autosomal recessive 15 (DFNB15)
(Deafness, autosomal recessive 72; DFNB72)
(Deafness, autosomal recessive 95; DFNB95)
3727 601884 Bone mineral density varitation quantitative trait locus 1 (BMND1)
(High bone mass; HBM, included)
(Osteoporosis, susceptibility to, included)
3728 601885 Cataract 14, multiple types (CTRCT14)
(Cataract, zonular pulverulent 3; CZP3)
(CAE3)
3729 601887 Malignant hyperthremia, susceptibility to, 5 (MHS5)
3730 601888 Malignant hyperthremia, susceptibility to, 6 (MHS6)
3731 601894 Glomerulopathy with fibronectin deposits 2 (GFND2)
(Glomerular nephritis, familial, with fibronectin deposits)
(Fibronectin glomerulopathy)
3732 601927 Lymphedema, cardiac septal defects, and characteristic facies
(Irons-Bianchi syndrome)
(Lymphedema, atrial septal defect, and characteristic facies)
3733 601941 Type 1 diabetes mellitus 6 (T1D6)
(Diabetes mellitus, insulin-dependent, 6; IDDM6)
(Insulin-dependent diabetes mellitus 6)
(Autoimmune thyroid disease, susceptibility to, 5, included; AITD5)
3734 601942 Type 1 diabetes mellitus 10 (T1D10)
(Diabetes mellitus, insulin-dependent, 10; IDDM10)
(Insulin-dependent diabetes mellitus 10)
3735 601952 Keratosis linearis with ichthyosis congenita and sclerosing keratoderma (KLICK)
(KLICK syndrome)
3736 601954 Muscular dystrophy, limb-girdle, autosomal recessive 7 (LGMDR7)
(Muscular dystrophy, limb-girdle, type 2G; LGMD2G)
3737 601957 Odontotrichoungual-digital-palmar syndrome
(OTUDP syndrome)
3738 601976 Otofacioosseous-gonadal syndrome




<facio osseous>
3739 601977 Thrombocythemia 2 (THCYT2)
3740 601979 Hyperzincemia with functional zinc depletion
3741 601992 Friedreich ataxia, type 2 (FRDA2)
3742 602014 Hypomagnesemia 1, intestinal (HOMG1)
(HOMG)
(Hypomagnesemia with secondary hypocalcemia; HSH)
(Hypomagnesemic tetany)
(Hypomagnesemia, intestinal, with secondary hypocalcemia)
3743 602032 Ectodermal dysplasia 4, hair/nail type (ECTD4)
(Ectodermal dysplasia, 'pure' hair/nail type)
3744 602066 Convulsions, familial infantile, with paroxysmal choreoathetosis (ICCA)
(Infantile convulsions and paroxysmal choreoathetosis, familial)
(ICCA syndrome)
(Paroxysmal kinesigenic dyskinesia with infantile convulsions; PKD/IC)
3745 602071 Broad terminal phalanges, familial
3746 602078 Fibrosis of extraocular muscles, congenital, 2 (CFEOM2)
(FEOM2 locus)
(Fibrosis of extraocular muscles, congenital, autosomal recessive)
3747 602079 Trimethylaminuria
(Fish-odor syndrome)
3748 602080 Paget disease of bone 2, early-onset (PDB2)
3749 602081 Speech-language disorder 1 (SPCH1)
(Childhood apraxia of speech; CAS)
(Developmental verbal dyspraxia)
(Speech and language disorder with orofacial dyspraxia)
3750 602082 Corneal dystrophy, Thiel-Behnke type (CDTB)
(Thiel-Behnke Corneal dystrophy; TBCD)
(Corneal dystrophy of Bowman layer, type II; CDB2)
(Corneal dystrophy, honeycomb-shaped)

前ページ 検索結果 9840件中3726-3750件目 次ページ