WormBase Tree Display for DO_term: DOID:14711
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| DOID:14711 | Name | FG syndrome | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A syndrome characterized by retardation, hyperactivity, hypotonia, broad thumbs, big first toes and a characteristic facial appearance including macrocephaly and has an X-linked recessive inheritance pattern. | ||||
| Comment | Xref MGI. | ||||
| Synonym | Exact | Keller syndrome | |||
| Opitz-Kaveggia syndrome | |||||
| Parent | Is_a | DOID:225 | |||
| DOID:0080012 | |||||
| DB_info | Database | OMIM | disease | 300321 | |
| 300406 | |||||
| 300422 | |||||
| 300581 | |||||
| 305450 | |||||
| Attribute_of | Gene_by_orthology | WBGene00001081 | |||
| WBGene00002991 |
