正常形態発生
形態発生の異常
異常形態発生の成因と発生機構
臨床診断の進め方
奇形診断の新しい検査
診断に役立つ文献とコンピュータを用いた診断支援システム
先天異常と社会
先天異常とバイオエシックス
発生予防の概念
先天異常発生要因への対応
出生前診断と胎児治療

Aarskog syndrome
Aase-Smith syndrome
acetoacetyl-CoA thiolase deficiency, mitochondrial
acheiropody
achondrogenesis
achondroplasia
acidemia, isovaleric, methylmalonic, propionic, argininosuccinic, glutaric
acoustic neuromata
acrocallosal syndrome (Schinzel type)
acrocephalopolydactylous dysplasia(Elejalde syndrome)
acrocephalopolysyndactyly
acrocephalosyndactyly
acrodysostosis
acrofacial dysostosis、 dysostosis, Nager type、dysostosis, postaxial type (postaxial dysostosis : POAD)
acromegaloid facial appearance syndrome、phenotype-cutis verticis gyrata-corneal leukoma
acromelic frontonasal dysostosis
acromesomelic dysplasia
acromicric dysplasia
acro-renal-mandibular syndrome
active ring X chromosome
acyl-CoA dehydrogenase deficiency (very-long-chain, long-chain, medium-chain, short-chain)，mitochondrial
adenine phosphoribosyltransferase deficiency
adenosine deaminase deficiency
adrenoleukodystrophy
agnathia-holoprosencephaly
agnathia-microstomia-synotia
Aicardi syndrome
albinism, Waardenburg type-Hirschsprung aganglionosis
Alexander disease
alopecia-anosmia-deafness-hypogonadism syndrome (Johnson type)
Alpers disease
Alzheimer disease, familial
amelo-cerebro-hypohidrotic syndrome
amelo-onycho-hypohidrotic syndrome
amniotic bands syndrome
amyloidoses
---中　略――
hypertelorism-hypospadias syndrome
hypertelorism-microtia-facial cleft-conductive deafness
hypervalinemia
hypochondroplasia
hypodontia-nail dysgenesis
hypoglossia-hypodactylia
hypogonadotropic hypogonadism
hypohidrotic ectodermal dysplasia, X-linked
hypomandibular faciocranial dysostosis
hypomelanosis of Ito, pigmentary dysplasia
hypoparathyroidism, familial
hypophosphatasia
hypophosphatemia, non X-linked, X-linked
hypopigmentation-immune defect, Griscelli type
hypospadias
hypothalamic hamartoblastoma syndrome, congenital, Hall-Pallister syndrome
hypoventilation, congenital central alveolar type
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