| D007231 |
Infant, Newborn |
An infant during the first 28 days after birth. |
Neonate,Newborns,Infants, Newborn,Neonates,Newborn,Newborn Infant,Newborn Infants |
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| D011247 |
Pregnancy |
The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. |
Gestation,Pregnancies |
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| D011656 |
Pulmonary Emphysema |
Enlargement of air spaces distal to the TERMINAL BRONCHIOLES where gas-exchange normally takes place. This is usually due to destruction of the alveolar wall. Pulmonary emphysema can be classified by the location and distribution of the lesions. |
Emphysema, Pulmonary,Centriacinar Emphysema,Centrilobular Emphysema,Emphysemas, Pulmonary,Focal Emphysema,Panacinar Emphysema,Panlobular Emphysema,Pulmonary Emphysemas,Centriacinar Emphysemas,Centrilobular Emphysemas,Emphysema, Centriacinar,Emphysema, Centrilobular,Emphysema, Focal,Emphysema, Panacinar,Emphysema, Panlobular,Emphysemas, Centriacinar,Emphysemas, Centrilobular,Emphysemas, Focal,Emphysemas, Panacinar,Emphysemas, Panlobular,Focal Emphysemas,Panacinar Emphysemas,Panlobular Emphysemas |
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| D012127 |
Respiratory Distress Syndrome, Newborn |
A condition of the newborn marked by DYSPNEA with CYANOSIS, heralded by such prodromal signs as dilatation of the alae nasi, expiratory grunt, and retraction of the suprasternal notch or costal margins, mostly frequently occurring in premature infants, children of diabetic mothers, and infants delivered by cesarean section, and sometimes with no apparent predisposing cause. |
Infantile Respiratory Distress Syndrome,Neonatal Respiratory Distress Syndrome,Respiratory Distress Syndrome, Infant |
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| D005260 |
Female |
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Females |
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| D006801 |
Humans |
Members of the species Homo sapiens. |
Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man |
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| D000328 |
Adult |
A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. |
Adults |
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| D059446 |
Heterotaxy Syndrome |
Abnormal thoracoabdominal VISCERA arrangement (visceral heterotaxy) or malformation that involves additional CONGENITAL HEART DEFECTS (e.g., heart isomerism; DEXTROCARDIA) and/or abnormal SPLEEN (e.g., asplenia and polysplenia). Irregularities with the central nervous system, the skeleton and urinary tract are often associated with the syndrome. |
Asplenia Syndrome,Asplenia with Cardiovascular Anomalies,Ivemark Syndrome,Left Atrial Isomerism,Left Atrial Isomerism with Polysplenia,Polysplenia Syndrome,Right Atrial Isomerism,Right Atrial Isomerism with Asplenia,Situs Ambiguus,Situs Ambiguus Viscerum,Situs Ambiguus with Asplenia,Situs Ambiguus with Polysplenia,Visceral Heterotaxy,Ambiguus Viscerum, Situs,Ambiguus Viscerums, Situs,Ambiguus, Situs,Asplenia Syndromes,Atrial Isomerism, Left,Atrial Isomerism, Right,Atrial Isomerisms, Left,Atrial Isomerisms, Right,Heterotaxies, Visceral,Heterotaxy Syndromes,Heterotaxy, Visceral,Isomerism, Left Atrial,Isomerism, Right Atrial,Isomerisms, Left Atrial,Isomerisms, Right Atrial,Left Atrial Isomerisms,Polysplenia Syndromes,Right Atrial Isomerisms,Situs Ambiguus Viscerums,Syndrome, Asplenia,Syndrome, Heterotaxy,Syndrome, Ivemark,Syndrome, Polysplenia,Syndromes, Asplenia,Syndromes, Heterotaxy,Syndromes, Polysplenia,Visceral Heterotaxies,Viscerum, Situs Ambiguus,Viscerums, Situs Ambiguus |
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