Seckel Syndrome
Disease ID: disease_node_20368
Connections displayed (default: 10).
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| Dbxref | GARD:8562, ICD10CM:Q87.1, MIM:PS210600, ORDO:808 |
|---|---|
| Subclassof | DOID_225, DOID_0050737 |
| Data Source | DOID |
| Synonyms | Harper's syndrome, Virchow-Seckel dwarfism, bird-headed dwarfism, microcephalic primordial dwarfism |
| Doid Label | Seckel syndrome |
| Doid Description | A syndrome characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability. Xref MGI. OMIM mapping confirmed by DO. [SN]. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_20368 |
| Doid Id | DOID_0050569 |
| Label | Seckel Syndrome |
- Incoming r'ship
SUBCLASS_OFto/from Seckel Syndrome 6(ID:disease_node_20374) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Syndrome(ID:disease_node_7213) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Seckel Syndrome 5(ID:disease_node_20369) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Seckel Syndrome 9(ID:disease_node_20375) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Seckel Syndrome 7(ID:disease_node_20370) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Seckel Syndrome 10(ID:disease_node_20373) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Seckel Syndrome 8(ID:disease_node_20372) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Seckel Syndrome 4(ID:disease_node_20371) (Disease)