| Metadata | |
|---|---|
| ID | DOID:0060468 |
| Name | Holt-Oram syndrome |
| Definition | A syndrome characterized by congenital anomalies located_in heart and located_in upper limb. http://ghr.nlm.nih.gov/condition/holt-oram-syndrome, https://en.wikipedia.org/wiki/Holt-Oram_syndrome, https://www.ncbi.nlm.nih.gov/pubmed/12223419, https://www.ncbi.nlm.nih.gov/pubmed/12436037 |
| Xrefs |
SNOMEDCT_US_2023_03_01:205814003 |
| Subsets |
DO_rare_slim NCIthesaurus |
| Synonyms |
atrio-digital syndrome [EXACT] atriodigital dysplasia [EXACT] heart-hand syndrome [EXACT] |
| Parent Relationships |
is_a autosomal dominant disease is_a syndrome |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance |