WormBase Tree Display for DO_term: DOID:3490
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| DOID:3490 | Name | Noonan syndrome | |
|---|---|---|---|
| Status | Valid | ||
| Definition | A RASopathy that is characterized by mildly unusual facial features, short stature, heart defects, bleeding problems, skeletal malformations, and many other signs and symptoms. | ||
| Comment | OMIM mapping confirmed by DO. | ||
| Synonym | Exact | Turner's phenotype, karyotype normal | |
| Parent | Is_a | DOID:0080690 | |
| DOID:0050177 | |||
| Child | Is (13) | ||
| Attribute_of | Gene_by_orthology | WBGene00001515 | |
| WBGene00002335 | |||
| WBGene00003030 | |||
| WBGene00004214 | |||
| WBGene00004947 | |||
| WBGene00005643 | |||
| WBGene00005644 | |||
| WBGene00005649 |
