Category
page 1Syndromes affecting head size
trichorhinophalangeal syndrome type II
Human disease
Macrocephaly-capillary malformation
disease
DeSanctis–Cacchione syndrome
rare autosomal recessive inherited syndrome. It is characterized by xeroderma pigmentosum, mental retardation, dwarfism, hypogonadism, and neurologic abnormalities
Okamoto syndrome
Autosomal dominant genetic condition
Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder
rare genetic disorder
Genitopatellar syndrome
medical condition