Heterotaxy, visceral, 12, autosomal is a condition characterized by abnormal arrangement of the internal organs, often involving complex congenital he...

Heterotaxy, visceral, 1, X-linked is a very rare condition characterized by abnormal arrangement of the internal thoracic and abdominal organs. This d...

Heterotaxy, visceral, 2, autosomal is a congenital condition affecting the normal left‐right arrangement of the internal organs, including the heart,...

Heterotaxy, visceral, 3, autosomal is a congenital condition characterized by an abnormal arrangement of the internal organs. This condition is presen...

Heterotaxy, visceral, 4, autosomal is a congenital condition that results in abnormal arrangement of the internal organs, particularly affecting the h...

Heterotaxy, visceral, 5, autosomal is a congenital condition in which the normal left-right asymmetry of internal organs is disrupted due to a mutatio...

Heterotopia, periventricular, associated with chromosome 5P anomalies is a condition affecting brain development, where clusters of neurons are abnorm...

Heterotopia, periventricular, X-linked dominant is a neurological condition characterized by abnormal neuronal migration and clustering of neurons alo...

Heyn-Sproul-Jackson syndrome is a rare condition sometimes referred to by its descriptive name: Microcephaly, Short Stature, and Impaired Intellectual...

HGSNAT-related retinopathy is an isolated eye condition caused by changes in the HGSNAT gene. These gene variants affect the normal function of the re...

HHV-6 encephalitis is a brain inflammation caused by an infection with the human herpesvirus 6. This condition can occur in people after an allogeneic...

Hibernoma is a benign, slow-growing tumor arising from brown adipose tissue and is most often observed in young adults. Recognized subtypes, such as c...