| D006984 |
Hypertrophy |
General increase in bulk of a part or organ due to CELL ENLARGEMENT and accumulation of FLUIDS AND SECRETIONS, not due to tumor formation, nor to an increase in the number of cells (HYPERPLASIA). |
Hypertrophies |
|
| D007223 |
Infant |
A child between 1 and 23 months of age. |
Infants |
|
| D008113 |
Liver Neoplasms |
Tumors or cancer of the LIVER. |
Cancer of Liver,Hepatic Cancer,Liver Cancer,Cancer of the Liver,Cancer, Hepatocellular,Hepatic Neoplasms,Hepatocellular Cancer,Neoplasms, Hepatic,Neoplasms, Liver,Cancer, Hepatic,Cancer, Liver,Cancers, Hepatic,Cancers, Hepatocellular,Cancers, Liver,Hepatic Cancers,Hepatic Neoplasm,Hepatocellular Cancers,Liver Cancers,Liver Neoplasm,Neoplasm, Hepatic,Neoplasm, Liver |
|
| D008297 |
Male |
|
Males |
|
| D009030 |
Mosaicism |
The occurrence in an individual of two or more cell populations of different chromosomal constitutions, derived from a single ZYGOTE, as opposed to CHIMERISM in which the different cell populations are derived from more than one zygote. |
|
|
| D002887 |
Chromosomes, Human, Pair 18 |
A specific pair of GROUP E CHROMOSOMES of the human chromosome classification. |
Chromosome 18 |
|
| D005315 |
Fetal Diseases |
Pathophysiological conditions of the FETUS in the UTERUS. Some fetal diseases may be treated with FETAL THERAPIES. |
Embryopathies,Disease, Fetal,Diseases, Fetal,Embryopathy,Fetal Disease |
|
| D006801 |
Humans |
Members of the species Homo sapiens. |
Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man |
|
| D000073842 |
Trisomy 18 Syndrome |
A chromosome disorder associated with TRISOMY of all or part of CHROMOSOME 18. Clinical manifestations include INTRAUTERINE GROWTH RETARDATION; CLEFT PALATE; CONGENITAL HEART DEFECTS; MICROCEPHALY; MICROGNATHIA and clenched fists with overlapping fingers. Most affected fetuses do not survive to birth. Those who survive through their first year often have severe INTELLECTUAL DISABILITY. |
Complete Trisomy 18 Syndrome,Edwards Syndrome,Mosaic Trisomy 18 Syndrome,Trisomy 18,Trisomy E Syndrome,Trisomy 18 Syndromes |
|
| D014314 |
Trisomy |
The possession of a third chromosome of any one type in an otherwise diploid cell. |
Partial Trisomy,Chromosomal Triplication,Chromosomal Triplications,Partial Trisomies,Trisomies,Trisomies, Partial,Trisomy, Partial |
|