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 |
検索結果 9743件中1-25件目 次ページ
| 項番 | 疾患No | 英語疾患名 |
|---|---|---|
| 1 | 100050 | Aarskog syndrome, autosoma dominant |
| 2 | 100070 | Aortic aneurysm, familial abdominal, 1 (AAA1) (Aneurysm, abdominal aortic; AAA) (Abdominal aortic aneurysm) |
| 3 | 100100 | Prune belly syndrome (PBS) (Absence of abdominal muscle with urinary tract abnormality and cryptorchidism) (Eagle-Barrett syndrome) [Early urethral obstruction sequence] |
| 4 | 100200 | Abducen palsy |
| 5 | 100300 | Adams-Oliver syndrome 1 (AOS1) (AOS) (Absence defect of limb, scalp and skull) (Congenital scalp defects with distal limb reduction anomalies) (Aplasia cutis congenita with terminal transverse limb defects) (Aplasia cutis congenita, congenital heart defect, and frontonasal cysts, included) |
| 6 | 100600 | Acanthosis nigricans |
| 7 | 100700 | Achard syndrome (Arachnodactyly-micrognathia) |
| 8 | 100800 | Achondroplasia (ACH) |
| 9 | 100820 | ACHOO syndrome (Autosomal dominant Compelling HelioOphthalmic Outburst syndrome) (Photic sneeze reflex) (Szeezing from light expose) (Peroutka sneeze) |
| 10 | 101000 | Neurofibromatosis, type II (NF2) (Neurofibromatosis, central type) (Acoustic schwannoma, bilateral) (Bilateral acoustic neurofibromatosis; BANF) (Acoustic neurinoma, bilateral; ACN) |
| 11 | 101120 | Acrocephalopolysyndactyly type III (ACPS III) (ACPS with leg hypoplasia) (Sakati-Nyhan syndrome) |
| 12 | 101200 | Apert syndrome (Acrocephalosyndactyly, type I; ACS1) (ACS I) (Apert-Crouzon syndrome, included) (Acrocephalosyndactyly, type II, included) (ACS II, included) (Vogt cephalodactyly, included) |
| 13 | 101400 | Saethre-Chotzen syndrome (SCS) (Acrocephalosyndactyly, type III; ACS3) (ACS III) (Chotzen syndrome) (Acrocephaly, skull asymmetry and mild syndactyly) (Saethre-Chotzen syndrome with eyelid anomalies, included) (Blepharophimosis, epicanthus inversus, and ptosis 3, formerly; BPES3, included) |
| 14 | 101600 | Pfeiffer syndrome (Acrocephalosyndactyly, type V; ACS5) (ASC V) (Noack syndrome) (Craniofacia-skeletal-dermatologic dysplasia, included) |
| 15 | 101800 | Acrodysostosis 1 with or without hormone resistance (ACRDYS1) |
| 16 | 101805 | Acrofacial dysostosis, Catania type (AFD, Catania type) |
| 17 | 101840 | Acrokeratoderma, hereditary papulo-translucent |
| 18 | 101850 | Keratoderma, palmoplantar, punctate type III (PPKP3) (Acrokeratoelastoidosis; AKE) (Collagenous plaques of hands and feet) |
| 19 | 101900 | Acrokeratosis verruciformis (AKV) (Hopf disease) |
| 20 | 102000 | Acroleukopathy, symmetric |
| 21 | 102100 | Acromegaloid changes, cutis vertcis gyrata, and corneal leukoma (Rosenthal-Kloepfer syndrome) |
| 22 | 102150 | Acromegaloid facial appearance syndrome (AFA syndrome) (Thick lips and oral mucosa) |
| 23 | 102200 | Pituitary adenoma 1, multiple types (PITA1) (Somatotrophinoma, familial isolated, FIS) (Isolated familian somatotropinosa; IFS) (Somatotrophinoma, familial) (Acromegaly due to pituitary adenoma 1) (PAGH1) (Pituitary adenoma predisposition, included; PAP) (Pituitary adenoma, familial isolated, included; FIPA) |
| 24 | 102200b | Acromegaly-pituitary tumor (Abbassioun 1986) |
| 25 | 102300 | Restless legs syndrome, susceptibility to, 1 (RLS1) (Acromelalgia, hereditary) (Ekbom syndrome) |
検索結果 9743件中1-25件目 次ページ