Human genes for IMAGe syndrome
IMAGe syndrome [DOID:0050885]
A syndrome that is characterized by intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, genital abnormalities and has_material_basis_in heterozygous mutation in the CDKN1C gene.
Synonyms: IMAGe syndrome, DOID:0050885, IMAGe disease, IMAGe disorder, IMAGe syndromes ...