Disease-gene associations mined from literature

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