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
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前ページ 検索結果 9793件中1026-1050件目 次ページ



項番 疾患No 英語疾患名
1026 164750 Omphalocele, autosomal
(Chromosome 1p31 duplication syndrome)
1027 164800 Nail disorder, nonsyndromic congenital, 5 (NDNCV)
(Onycholysis, partial with scleronychia)
(Onycholysis, hereditary distal)
1028 164900 Ophthalmomandibulomelic dysplasia
(OMM syndrome)
[Pillary syndrome]
1029 165000 Ophthalmoplegia, familial static
(External ophthalmoplegia, nonprogressive, congenital hereditary)
1030 165098 Ophthalmoplegia, familial total, with iris transillumination
1031 165150 Ophthalmoplegia, progressive, with scrotal tongue and mental deficiency
1032 165199 Optic atrophy, hearing loss, and peripheral neuropathy, autosomal dominant
1033 165200 Optic atrophy with demyelinating disease of CNS
1034 165300 Optic atrophy 3, autosomal dominant (OPA3)
(Optic atrophy and cataract, autosomal dominant)
1035 165500 Optic atrophy 1 (OPA1)
(Optic atrophy, juvenile)
(Kjer-type Optic atrophy)
(Optic atrophy, Kjer type; OAK)
1036 165510 Optic atrophy 13 with retinal and foveal abnormalities (OPA13)
(Optic atrophy with negative electoretinograms, formerly)
1037 165550 Optic nerve hypoplasia, familial bilateral
(Optic nerve aplasia, bilateral, included)
1038 165590 Orofaciodigital syndrome X (OFD10)
(OFDS X)
(Oral-facial-digital syndrome, type X)
(Orofaciodigital syndrome with fibular aplasia)
(Oral-facial-digital syndrome with fibular aplasia)
1039 165600 Orbital margin, hypoplasia of
1040 165660 OSLAM syndrome
(Osteosarcoma, limb anomalies, and macrocytosis)
(OSteosarcoma, Limb Anomalies, erythroid Macrocytosis with megaloblastic marrow)
1041 165670 Ossified ear cartilages
1042 165680 Ossicular malformations, familial
(Auditory ossicle malformation (autosomal dominant))
1043 165700 Thiemann disease
(Thiemann epiphyseal disease)
(Osteoarthropathy of fingers, familial)
1044 165720 Osteoarthritis susceptibility 1 (OS1)
(OA)
(Osteoarthrosis)
(Osteoarthritis of hip, female-specific, susceptibility to)
1045 165800 Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans (SSOAOD)
1046 166000 Enchondromatosis, multiple, Ollier type
(Ollier disease)
(Osteochondromatosis)
(Dyschondroplasia)
1047 166200 Osteogenesis imperfecta, type I (OI1)
(OI, type I)
(Osteogenesis imperfecta tarda)
(Osteogenesis imperfecta with blue sclerae)
(Osteopenic nonfracture syndrome, included)
1048 166210 Osteogenesis imperfecta, type II (OI2)
(OI, type II)
(Osteogenesis imperfecta congenita, perinatal lethal form)
(Osteogenesis imperfecta congenita; OIC)
(Vrolick type of osteogenesis imperfecta)
1049 166220 Osteogenesis imperfecta, type IV (OI4)
(OI, type IV)
(OI4)
(Osteogenesis imperfecta with normal sclerae)
1050 166230 Osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones, but without fractures

前ページ 検索結果 9793件中1026-1050件目 次ページ