Lissencephaly
Disease ID: disease_node_11852
Connections displayed (default: 10).
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| Dbxref | GARD:12291, ICD10CM:Q04.3, MESH:D054082, MIM:PS607432, NCI:C103921, ORDO:102009, SNOMEDCT_US_2023_03_01:204036008, SNOMEDCT_US_2023_03_01:23024003, UMLS_CUI:C0266463, UMLS_CUI:C0266483 |
|---|---|
| Subclassof | DOID_2490 |
| Data Source | DOID, MESH |
| Disease Has Location | UBERON_0000956 |
| Mesh Id | D054082 |
| Mesh Label | Lissencephaly |
| Mesh Subclassof | D054081 |
| Doid Label | lissencephaly |
| Doid Description | A congenital nervous system abnormality characterized by the absence of folds in the cerebral cortex and caused_by defective neuronal migration during the 12th to 24th weeks of gestation. Xref MGI. OMIM mapping confirmed by DO. [SN]. |
| Disease Node Id | disease_node_11852 |
| Doid Id | DOID_0050453 |
| Label | Lissencephaly |
- Incoming r'ship
SUBCLASS_OFto/from X-Linked Lissencephaly 2(ID:disease_node_19265) (Disease) - Incoming r'ship
SUBCLASS_OFto/from X-Linked Lissencephaly 1(ID:disease_node_19264) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Pachygyria, Microcephaly, Developmental Delay, And Dysmorphic Facies, With Or Without Seizures(ID:disease_node_19275) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Lissencephaly 10(ID:disease_node_19273) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Lissencephaly 1(ID:disease_node_19266) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Lissencephaly 9 With Complex Brainstem Malformation(ID:disease_node_19274) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Lissencephaly 7 With Cerebellar Hypoplasia(ID:disease_node_19271) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Lissencephaly 5(ID:disease_node_19272) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Microlissencephaly(ID:disease_node_19267) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Lissencephaly 8(ID:disease_node_19270) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Congenital Nervous System Abnormality(ID:disease_node_13582) (Disease)