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
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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