Contains stomach, intestines, spleen, and liver, and other organs
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adenocarcinoma
cancerous tumor of glandular tissue
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adenoma
tumor of a gland
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anaplasia
a change in the structure of cells and in their orientation to each other
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anatomy
The study of body structure
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anomaly
deviation from what is normal
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anterior
front
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aplasia
lack of development
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atresia
absence of normal body opening
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autopsy
the examination of a corpse to determine the cause of death
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bloodborne transmission
the spread of a disease through contact with blood or other body fluids that are contaminated with blood
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caudal
toward the tail
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cephalic
pertaining to the head
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chromosome
a threadlike structure of nucleic acids and protein found in the nucleus of most living cells, carrying genetic information in the form of genes.
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communicable disease
a disease that is spread from one host to another
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congenital disorder
an abnormal condition that exists at the time of birth
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cytoplasm
A jellylike fluid inside the cell in which the organelles are suspended
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distal
away from the point of attachment
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dorsal
back
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dysplasia
abnormal development
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endemic
A disease that is particular to a locality or region.
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endocrine glands
Glands of the endocrine system that release hormones into the bloodstream
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epidemic
A widespread outbreak of an infectious disease.
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epigastric region
located above the stomach
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etiology
cause of disease
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exocrine glands
secrete chemical substances into ducts that lead either to other organs or out of the body
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functional disorder
produces symptoms for which no physiological or anatomical cause can be identified
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genetic disorder
An abnormal condition that a person inherits through genes or chromosomes
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geriatrician
a physician who specializes in the care of older people
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hemophilia
A hereditary disease where blood does not coagulate to stop bleeding
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histology
study of tissues
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homeostasis
A tendency to maintain a balanced or constant internal state; the regulation of any aspect of body chemistry, such as blood glucose, around a particular level
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hyperplasia
increase in number of cells
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hypertrophy
increase in muscle size
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hypogastric region
located below the stomach
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hypoplasia
incomplete development of an organ or tissue
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iatrogenic illness
an unfavorable response due to prescribed medical treatment
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idiopathic disease
a disease that develops without a known or apparent cause
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infectious disease
an illness caused by living pathogenic organisms such as bacteria and viruses
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inguinal
groin
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medial
toward the midline
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messentery
fine peritoneal membrane that holds in place the coils of the small intestine
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midsagittal plane
divides the body into equal right and left halves
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nosocomial infection
an infection acquired during hospitalization
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pandemic
worldwide epidemic
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pathology
study of disease
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pelvic cavity
Contains urinary bladder, reproductive organs, and rectum
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peritoneum
membrane that lines the abdominal cavity
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peritonitis
inflammation of the peritoneum
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physiology
The study of body function
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posterior
toward the back
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proximal
Closer to the point of attachment
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retroperitoneal
located behind the peritoneum
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stem cells
unspecialized cells that are able to renew themselves for long periods of time by cell division
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syndrome
a group of symptoms
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thoracic cavity
contains heart and lungs
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transverse plane
horizontal division of the body into upper and lower portions
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umbilicus
depression on the abdomen marking site of entry of umbilical cord
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vector-borne transmission
the spread of certain disease due to the bite of a vector
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ventral
belly side
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saggital plane
divides the body into left and right halves
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coronal (frontal) plane
vertical division of the body into front (anterior) and back (posterior) portions
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-poietic
formation
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genetic disorder (hereditary disease)
a pathological condition caused by an absent or defective gene
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cystic fibrosis
A genetic disorder that is present at birth and affects both the respiratory and digestive systems.
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down syndrome
a condition of intellectual disability and associated physical disorders caused by an extra copy of chromosome 21.
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fragile x syndrome
a disorder produced by injury to a gene on the X chromosome, producing mild to moderate mental retardation
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Huntington's disease
A human genetic disease caused by a dominant allele; characterized by uncontrollable body movements and degeneration of the nervous system
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marfan syndrome
autosomal dominant; pleiotropic; tall, weak heart
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muscular dystrophy
group of hereditary diseases characterized by degeneration of muscle and weakness
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phenylketonuria
a genetic disorder in which the essential digestive enzyme phenylalanine hydroxylase is missing
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adenitis
inflammation of a gland
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adenosis
abnormal condition of a gland
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postmortem
after death
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health care proxy
a person chosen by another person to make medical decisions if the second person becomes unable to do so
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living will
A document that indicates what medical intervention an individual wants if he or she becomes incapable of expressing those wishes.
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DNR
do not resuscitate
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general practitioner
a physician who diagnoses and treats a variety of common health problems
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internist
a physician who specializes in diagnosing and treating diseases and disorders of the internal organs and related body systems