hypoplasia of the body

См. также в других словарях:

• hypoplasia — [hī΄pō plā′zhə] n. [ModL < HYPO + PLASIA] a condition of decreased or arrested growth of an undeveloped organ or tissue of the body hypoplastic [hī΄pōplas′tik] adj …   English World dictionary

• Optic nerve hypoplasia — Classification and external resources ICD 10 Q07.81 ICD 9 377.43, 743.57 …   Wikipedia

• X-linked adrenal hypoplasia congenita — Classification and external resources OMIM 300200 DiseasesDB 32988 X linked adrenal hypoplasia congenita is a genetic dis …   Wikipedia

• Cat body type genetic mutations — Cats, like all living organisms, occasionally have mutations that affect their body type. Sometimes, these changes in body type are striking enough that humans select for and perpetuate them. This is not always in the best interests of the cat,… …   Wikipedia

• Agenesis of the corpus callosum — Classification and external resources OMIM 217990 DiseasesDB 29900 eMedicine …   Wikipedia

• syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… …   Medical dictionary

• Bioarchaeology — The term bioarchaeology was first coined by British archaeologist Grahame Clark in 1972 as a reference to zooarchaeology, or the study of animal bones from archaeological sites. Redefined in 1977 by Jane Buikstra, bioarchaeology in the US now… …   Wikipedia

• Anemia — The condition of having less than the normal number of red blood cells or less than the normal quantity of hemoglobin in the blood. The oxygen carrying capacity of the blood is, therefore, decreased. Persons with anemia may feel tired and fatigue …   Medical dictionary

• Achondroplasia — The most common form of short stature with disproportionately short limbs dwarfism with short arms and legs. Achondroplasia is caused by mutation in the fibroblast growth factor receptor 3 gene (FGFR3), which is located on chromosome 4 in… …   Medical dictionary

• Congenital heart defect — Classification and external resources The normal structure of the heart (left) in comparison to two common locations for a ventricular septal defect (right), the most common form of congenital heart defect.[1] …   Wikipedia

• Androgen insensitivity syndrome — Classification and external resources AIS results when the function of the androgen receptor (AR) is impaired. The AR protein (pictured) mediates the effects of androgens in the human body. ICD 10 E …   Wikipedia