is a rare genetic condition that can affect growth and feeding.

occurs when both copies of chromosome 21 come from the mother.

happens when both copies of chromosome 22 come from the mother.

happens when both copies of chromosome 4 come from the mother.

happens when both chromosome 6 copies come from the mother.

is when both chromosome 9 copies come from the mother.

is when both X chromosomes come from the mother.

is an inherited mitochondrial condition causing diabetes and hearing loss.

is a rare genetic condition affecting eye development and several organs.

is a cancer of mature B cells, the white blood cells.

is an advanced lens opacity causing severe, painless vision loss.

is a rare, usually benign stomach tumor containing different body tissues.

is a rare cancer of mature T cells or NK cells.

is a usually noncancerous tumor made of mature body tissues.

is a usually noncancerous ovarian tumor made of mature body tissues.

is an inherited, early-onset diabetes from HNF4A variants, often tablet-treatable.

is an inherited form of diabetes caused by changes in INS gene.

is a rare inherited form of diabetes often starting in youth.

is an inherited diabetes caused by KCNJ11 gene changes, often starting young.

is a rare inherited form of diabetes that usually begins young.

is a hereditary, mild diabetes causing lifelong fasting high blood sugar (hyperglycemia).

is a genetic HNF1A-related diabetes causing early-onset hyperglycemia.

is a rare inherited form of diabetes that usually develops in youth.

is a rare inherited form of diabetes often linked to kidney problems.