[{"n": "1p36 deletion syndrome", "u": "/e/genetic-anomalies/1p36-deletion-syndrome/", "s": "A genetic deletion syndrome affecting development, behavior, and multiple organ systems."}, {"n": "2p15-16.1 microdeletion syndrome", "u": "/e/genetic-anomalies/2p15-16-1-microdeletion-syndrome/", "s": "Rare genetic syndrome from a small chromosome 2 deletion."}, {"n": "3p deletion syndrome", "u": "/e/genetic-anomalies/3p-deletion-syndrome/", "s": "Rare genetic disorder from deletion of chromosome 3p arm."}, {"n": "17q12 microdeletion syndrome", "u": "/e/genetic-anomalies/17q12-microdeletion-syndrome/", "s": "A rare genetic syndrome linked to kidney disease and neuropsychiatric conditions."}, {"n": "22q11.2 distal deletion syndrome", "u": "/e/genetic-anomalies/22q11-2-distal-deletion-syndrome/", "s": "A rare genomic disorder from a missing chromosome 22 segment."}, {"n": "22q11.2 duplication syndrome", "u": "/e/genetic-anomalies/22q11-2-duplication-syndrome/", "s": "A rare genetic disorder with variable symptoms and frequent inheritance from normal parents."}, {"n": "Chimera (genetics)", "u": "/e/genetic-anomalies/chimera-genetics/", "s": "Single organism with cells of different genotypes."}, {"n": "DiGeorge syndrome", "u": "/e/genetic-anomalies/digeorge-syndrome/", "s": "Genetic disorder from 22q11.2 deletion, affecting heart, immune system, and development."}, {"n": "Fragile X-associated primary ovarian insufficiency", "u": "/e/genetic-anomalies/fragile-x-associated-primary-ovarian-insufficiency/", "s": "Genetic condition causing premature ovarian failure in FMR1 premutation carriers."}, {"n": "Genetic incompatibility", "u": "/e/genetic-anomalies/genetic-incompatibility/", "s": "Genetic mismatches reduce offspring viability and shape mating strategies."}, {"n": "Human chimera", "u": "/e/genetic-anomalies/human-chimera/", "s": "A human with two distinct genotypes in one body."}, {"n": "Intersex (biology)", "u": "/e/genetic-anomalies/intersex-biology/", "s": "Organisms with sex characteristics between male and female."}, {"n": "Klinefelter syndrome", "u": "/e/genetic-anomalies/klinefelter-syndrome/", "s": "A chromosome anomaly causing infertility and small testicles in males."}, {"n": "Koolen–De Vries syndrome", "u": "/e/genetic-anomalies/koolen-de-vries-syndrome/", "s": "Rare genetic disorder from 17q21.31 microdeletion, discovered in 2006."}, {"n": "Mosaic variegated aneuploidy syndrome", "u": "/e/genetic-anomalies/mosaic-variegated-aneuploidy-syndrome/", "s": "Rare genetic disorder causing mosaic aneuploidy and congenital abnormalities."}, {"n": "Müllerian anomalies", "u": "/e/genetic-anomalies/m-llerian-anomalies/", "s": "Congenital malformations of the female reproductive tract from embryonic development errors."}, {"n": "Prader–Willi syndrome", "u": "/e/genetic-anomalies/prader-willi-syndrome/", "s": "A rare genetic disorder causing insatiable hunger and developmental challenges."}, {"n": "Ring chromosome 22", "u": "/e/genetic-anomalies/ring-chromosome-22/", "s": "Rare chromosomal disorder with variable phenotype and SHANK3 deletion."}, {"n": "Smith–Magenis syndrome", "u": "/e/genetic-anomalies/smith-magenis-syndrome/", "s": "A microdeletion syndrome with distinct facial, sleep, and behavioral features."}]