DO_rare_slim NCIthesaurus has material basis in has phenotype has symptom autosomal recessive disease Dubowitz syndrome ICD10CM:Q87.19 SNOMEDCT_US_2025_09_01:2593002 MIM:223370 MESH:C535718 A syndrome that is characterized by microcephaly, growth retardation and a characteristic facial appearance including but not limited to narrow or triangular shaped head, micrognathia, ptosis, a broad, wide-tipped nose, and wide-set eyes with drooping eyelids. disease_ontology MEDDRA:10059589 UMLS_CUI:C0175691 DOID:14796 Dubowitz's syndrome NCI:C125591 GARD:6290 OMIM mapping confirmed by DO. [SN]. syndrome autosomal recessive inheritance Retrognathia Growth delay ptosis