Abnormalities, Multiple
Also known asMultiple Abnormalities
Definition
Congenital abnormalities that affect more than one organ or body structure.
MeSH classification
- C16.131.077
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22q11 Deletion Syndrome
Condition with a variable constellation of phenotypes due to deletion polymorphisms at chromosome location 22q11. It encompasses several syn…
46, XX Disorders of Sex Development
Congenital conditions in individuals with a female karyotype, in which the development of the gonadal or anatomical sex is atypical.
46, XX Testicular Disorders of Sex Development
Congenital conditions in individuals in which male GONADS develop in a genetic female (female to male sex reversal).
Abnormalities, Drug-Induced
Congenital abnormalities caused by medicinal substances or drugs of abuse given to or taken by the mother, or to which she is inadvertently …
Abnormalities, Radiation-Induced
Congenital changes in the morphology of organs produced by exposure to ionizing or non-ionizing radiation.
Abnormalities, Severe Teratoid
Marked developmental anomalies of a fetus or infant.
Acrocallosal Syndrome
Autosomal recessive syndrome characterized by hypogenesis or agenesis of CORPUS CALLOSUM. Clinical features include MENTAL RETARDATION; CRAN…
Acrocephalosyndactylia
Congenital craniostenosis with syndactyly.
Source: NIH MeSH 2026 (D000015) — National Library of Medicine, public domain. View official MeSH record ↗