WordNet

moderate in type or degree or effect or force; far from extreme; "a mild winter storm"; "a mild fever"; "fortunately the pain was mild"; "a mild rebuke"; "mild criticism"
a Cypriot monetary unit equal to one thousandth of a pound
a unit of length equal to one thousandth of an inch; used to specify thickness (e.g., of sheets or wire)
an angular unit used in artillery; equal to 1/6400 of a complete revolution
the syllable naming the third (mediant) note of any major scale in solmization
abnormal development (of organs or cells) or an abnormal structure resulting from such growth

PrepTutorEJDIC

(人,人の気性・態度などが)『柔和な』,ものやわらかな,温和な / (程度・力・効果などが)『適度な』,ほどよい / (病気などが)そんなにひどくない,軽い / (気温が)おだやかな / (味・においが)強くない,ぴりぴりしない
マイルド(苦みの少ないビールの一種)
ミル(1000分の1インチ)
ミ(全音階の第3音)

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1. 先天性股関節脱臼：治療および転帰 developmental dysplasia of the hip treatment and outcome
2. 先天性股関節脱臼：臨床的特徴および診断 developmental dysplasia of the hip clinical features and diagnosis
3. 遺伝性皮膚症 the genodermatoses
4. 歯の発達障害 developmental defects of the teeth
5. 気管支肺異形成症を有する乳児の転帰 outcome of infants with bronchopulmonary dysplasia

The diagnostic challenge of progressive pseudorheumatoid dysplasia (PPRD): A review of clinical features, radiographic features, and WISP3 mutations in 63 affected individuals.

Garcia Segarra N, Mittaz L, Campos-Xavier AB, Bartels CF, Tuysuz B, Alanay Y, Cimaz R, Cormier-Daire V, Di Rocco M, Duba HC, Elcioglu NH, Forzano F, Hospach T, Kilic E, Kuemmerle-Deschner JB, Mortier G, Mrusek S, Nampoothiri S, Obersztyn E, Pauli RM, Selicorni A, Tenconi R, Unger S, Utine GE, Wright M, Zabel B, Warman ML, Superti-Furga A, Bonafé L.SourceDivision of Molecular Pediatrics, Lausanne University Hospital, Lausanne, Switzerland.
American journal of medical genetics. Part C, Seminars in medical genetics.Am J Med Genet C Semin Med Genet.2012 Aug 15;160(3):217-29. doi: 10.1002/ajmg.c.31333. Epub 2012 Jul 12.
Progressive pseudorheumatoid dysplasia (PPRD) is a genetic, non-inflammatory arthropathy caused by recessive loss of function mutations in WISP3 (Wnt1-inducible signaling pathway protein 3; MIM 603400), encoding for a signaling protein. The disease is clinically silent at birth and in infancy. It ma
PMID 22791401

Terhal PA, van Dommelen P, Le Merrer M, Zankl A, Simon ME, Smithson SF, Marcelis C, Kerr B, Kinning E, Mansour S, Hennekam RC, van der Hout AH, Cormier-Daire V, Lund AM, Goodwin L, Mégarbané A, Lees M, Betz RC, Tobias ES, Coucke P, Mortier GR.SourceDepartment of Biomedical Genetics, University Medical Centre Utrecht, Utrecht, The Netherlands. p.a.terhal@umcutrecht.nl.
American journal of medical genetics. Part C, Seminars in medical genetics.Am J Med Genet C Semin Med Genet.2012 Aug 15;160(3):205-16. doi: 10.1002/ajmg.c.31332. Epub 2012 Jul 12.
From data collected via a large international collaborative study, we have constructed a growth chart for patients with molecularly confirmed congenital spondylo-epiphyseal dysplasia (SEDC) and other COL2A1 related dysplasias. The growth chart is based on longitudinal height measurements of 79 patie
PMID 22791362

Histological Comparison of Long-Bone Cortex between 11-Year-Old Giant Cow with Dermal Dysplasia and the Child Cow Aged 8.5 Years

MORI Ryoichi,KODAKA Tetsuo,NAITO Yoshihisa
Journal of Veterinary Medical Science advpub(0), 1109020624, 2011
… Previously, we reported that an 11-year-old giant Holstein cow with dermal dysplasia showed a delayed osteon formation. … An 8.5-year-old cow, born from the giant Holstein cow, also showed some dermal dysplasia and the outer-half layer of the child almost retained laminar bone similar to that of the mother, although the body weight was approximately normal. …
NAID 130001032966

G9M.139 医学事典