| Metadata | |
|---|---|
| ID | DOID:0060408 |
| Name | chromosome 19q13.11 deletion syndrome |
| Definition | A chromosomal deletion syndrome that has_material_basis_in a chromosome 19q13.11 deletion and that is characterized by characterized by poor overall growth, slender habitus, microcephaly, delayed development, intellectual disability with poor or absent speech, and feeding difficulties. https://pubmed.ncbi.nlm.nih.gov/24243649 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
19q13.11 microdeletion syndrome [EXACT] monosomy 19q13.11 [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance |