Temple syndrome (DOID:0111713)
Alliance: disease page
Alt IDs: OMIM:616222, NCI:C120409, ORDO:254516, UMLS_CUI:C4015558
Definition: 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.