Kikuchi-Fujimoto disease is a benign, self-limited condition primarily characterized by tender regional cervical lymphadenopathy accompanied by mild f...

Kilquist syndrome is a rare genetic condition that affects multiple systems in the body. It is an autosomal recessive disorder, which means that two c...

Kimura disease is a chronic, benign inflammatory condition that mainly appears in Asian countries and mostly affects young men. It typically shows up...

Kindler syndrome (KS) is a rare inherited condition that is part of the epidermolysis bullosa group, which also includes the simplex, junctional, and...

King-Denborough syndrome is a rare genetic disorder that affects the muscles and the development of certain body features. It is known as a genetic no...

KIZ-related retinopathy is a type of retinal disease caused by changes in the KIZ gene. The condition affects the retina, an important part of the eye...

Kleefstra syndrome is a neurodevelopmental disorder primarily characterized by intellectual disability, childhood hypotonia, severe delays in expressi...

Kleefstra syndrome 1 is an autosomal dominant condition characterized by intellectual disability, distinctive facial features, and neurological challe...

Kleefstra syndrome 2, also known as KLEFS2, is a rare genetic condition that is linked to changes in the KMT2C gene. It is referenced in important med...

Information about the overall nature of this condition is currently limited for this condition. Kleefstra syndrome due to 9q34 microdeletion is a rare...

Information about the overview of Kleefstra syndrome due to a point mutation is currently limited. This condition is registered in well-known rare dis...

Kleine-Levin syndrome is a rare neurological disorder characterized by relapsing-remitting episodes of excessive sleepiness along with cognitive and b...

Information about overview is currently limited for this condition.

Information about overview is currently limited for this condition.

KLHL9-related early-onset distal myopathy is a rare genetic condition that affects the muscles, particularly those in the distal parts of the limbs. I...

Klinefelter syndrome is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome (also known as KFS4) is a rare condition that appears to affect the development of the bones...

Klippel-Feil syndrome is a congenital musculoskeletal condition where at least two of the neck vertebrae are fused together. This fusion can lead to a...

Klippel-Feil syndrome 1, autosomal dominant is a rare condition that occurs because of a mutation in the GDF6 gene. This condition is described as an...

Klippel-Feil syndrome 2, autosomal recessive is a type of isolated Klippel-Feil syndrome that is caused by a mutation in the MEOX1 gene. This conditio...