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MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Defects in certain proteins cause major heart abnormalities during early development.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

Early sexual development in children, especially girls, can be treated with hormone therapy to improve adult height and requires support for the child and family.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

Stem cells compete for space using cell adhesion, and mutations can affect their competitive success, with implications for tissue health and disease.

Excluding alopecia and mucous membrane components from the CLASI-A score reduces its effectiveness in capturing important disease activity.

Root hairs help Arabidopsis plants absorb more phosphorus when it's scarce.

Cell adhesion molecules are important in the development of certain skin diseases.

FOXN1 mutations can cause varying immune and physical issues, with severity influenced by gene activity and possibly other factors.

ACTH promotes hair growth in mink, but α-MSH does not.

MT-DADMe-ImmA can selectively kill head and neck cancer cells without harming normal cells.

Copper supplements during pregnancy improve survival and development in mutant mice.

Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

Mite infestations severely harm the health of endangered Amargosa voles.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

Psoriasis may be chronic because it lacks certain immune system controls that prevent overreaction.

Three siblings had both Vohwinkel's disease and congenital alopecia, with no effective treatment.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

A newborn with severe low blood sugar due to a genetic issue needed major surgery after standard treatments failed.

Early over-expression of FoxN1 harms immune and skin development.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

Living with metastatic pancreatic cancer involves symptoms like fatigue and nausea, and impacts like anxiety and reduced physical function.

Indralupta, similar to Alopecia Areata, is caused by an imbalance of body energies, leading to patchy hair loss.

Wild African goats have genetic adaptations for surviving harsh desert conditions.

Selenium imbalance can cause hair loss and skin issues.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

Stress likely causes hair loss in Formosan macaques.