Human genes for Temple syndrome
Temple syndrome [DOID:0111713]
A syndrome characterized by low birth weight, hypotonia and motor delay, feeding problems early in life, early puberty, and significantly reduced final height that has_material_basis_in heterozygous mutation in an impriniting region on chromosome 14q32.
Synonyms: Temple syndrome, DOID:0111713, Temple disease, Temple disorder, Temple syndromes