Carey-Fineman-Ziter Syndrome
Disease ID: disease_node_20301
Connections displayed (default: 10).
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| Dbxref | MIM:254940 |
|---|---|
| Subclassof | DOID_225 |
| Data Source | DOID |
| Doid Label | Carey-Fineman-Ziter syndrome |
| Doid Description | A syndrome characterized by hypotonia, Moebius sequence (bilateral congenital facial palsy with impairment of ocular abduction), Pierre Robin complex (micrognathia, glossoptosis, and high-arched or cleft palate), delayed motor milestones, and failure to thrive. |
| Has Symptom | SYMP_0000369 |
| Disease Node Id | disease_node_20301 |
| Doid Id | DOID_0080194 |
| Label | Carey-Fineman-Ziter Syndrome |
- Outgoing r'ship
HAS_SYMPTOMto/from Blepharoptosis(ID:disease_node_1612) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Syndrome(ID:disease_node_7213) (Disease)