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2276-2300件目 次ページ



項番 疾患No 英語疾患名
2276 242300 Ichthyosis, congenital, autosomal recessive 1 (ARCI1)
(Ichthyosis, congenital, autosomal recessive 1, with bathing suit distribution)
(Collodion baby, self-healing; SHCB)
(Ichthyosis congenita)
(Lamellar exforiation of newborn)
(Desquamation of newborn)
(Collodion fetus)
(Ichthyosis congenita II; ICR2)
(Ichthyosis, lamellar, 1, formerly; LI1)
2277 242400 Ichthyosis congenita with biliary atresia
2278 242500 Ichthyosis, congenital, autosomal recessive 4B (ARCI4B)
(Ichthyosis congenita, Harlequin fetus type)
(Harlequin ichthyosis)
(Harlequin fetus)
2279 242510 Ichthyosis with alopecia, eclabion, ectropion, and mental retardation
2280 242520 Ichthyosis, hepatosplenomegaly, cerebellar degeneration
2281 242530 Ichthyosis, mental retardation, dwarfism, renal impairment
2282 242550 Ichthyosis, split hairs and aminoaciduria
2283 242600 Iminoglycinuria
2284 242670 Immotile cilia syndrome due to defective radial spokes
2285 242680 Ciliary dyskinesia with excessively long cilia
(Immotile cilia syndrome due to excessive long cilia)
2286 242700 T-lymphocyte deficiency with thymic aplasia (TIDTA)
(Immune defect due to absence of thymus)
(T-lymphocyte deficiency)
(Nezelof syndrome)
2287 242840 Vici syndrome
(Immunodeficiency with cleft lip/palate, cataracts, hypopigmentation, and absent corpus callosum)
2288 242850 Immune deficiency disease
2289 242860 Immunodeficiency-centromeric instability-facial anomalies syndrome 1
(ICF1)
(Immunodeficiency, variable, with centromeric instability of chromosomes 1, 9, and 16)
(Centromeric instability, immunodeficiency syndrome; CIID)
(Immunodeficiency syndrome, variable)
2290 242870 Immunodeficiency, partial combined, with absence of HLA determinants and beta-2-microglobulin lymphocytes
2291 242880 Immunoerythromyeloid hypoplasia
2292 242890 Immunoglobulin D level in plasma, low
2293 242900 Schimke immunoosseous dysplasia (SIOD)
(Immunoosseous dysplasia, Schimke type)
2294 243000 Indifference to pain, congenital, autosomal recessive (CIP)
(Insensitivity to pain, channelopathy-associated)
(Congenital analgesia, autosomal recessive)
(Asymbolia for pain)
(Neuropathy, hereditary sensory and autonomic, type IID, included; HSAN2D)
2295 243050 Indolylacroyl glycinemia with mental retardation
2296 243060 Spermatogenic failure 5 (SPGF5)
(Male infertility with large-headed, multiflagellar, polyploid spermatozoa)
(Infertility associated with multi-tailed spermatozoa and excessive DNA)
2297 243080 Inosine phosphorylase deficiency, immune defect due to
2298 243100 Internal carotid arteries, hypoplasia of
2299 243110 Immunodeficiency with defective T-cell response to interleukin 1
(Interleukin 1, defective T-cell response to)
2300 243150 Gastrointestinal defects and immunodeficiency syndrome (GIDID)
(Intestinal atresia, multiple and/or inflammatory bowel disease with or without immunodeficiency)
(Intestinal atresia, multiple ; MINAT)
(Familial intestinal polyatresia syndrome; FIPA)

前ページ 検索結果 9840件中2276-2300件目 次ページ