Chromosomal Deletion Syndrome
Disease ID: disease_node_15239
Connections displayed (default: 10).
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| Subclassof | DOID_0080014 |
|---|---|
| Data Source | DOID |
| Doid Label | chromosomal deletion syndrome |
| Doid Description | A chromosomal disease that has_material_basis_in partial deletion of chromosomes. |
| Disease Node Id | disease_node_15239 |
| Doid Id | DOID_0060388 |
| Label | Chromosomal Deletion Syndrome |
- Incoming r'ship
SUBCLASS_OFto/from Y-Linked Spermatogenic Failure 1(ID:disease_node_15238) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Williams Syndrome(ID:disease_node_9850) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Wagr Syndrome(ID:disease_node_9254) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Wolf-Hirschhorn Syndrome(ID:disease_node_11984) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Smith-Magenis Syndrome(ID:disease_node_12534) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Rubinstein-Taybi Syndrome(ID:disease_node_6709) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Phelan-Mcdermid Syndrome(ID:disease_node_17088) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Hereditary Nonpolyposis Colorectal Cancer Type 8(ID:disease_node_17089) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Jacobsen Distal 11Q Deletion Syndrome(ID:disease_node_11980) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Digeorge Syndrome(ID:disease_node_2526) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Cri-Du-Chat Syndrome(ID:disease_node_2308) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chromosome 6Q24-Q25 Deletion Syndrome(ID:disease_node_17099) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chromosome 6Q11-Q14 Deletion Syndrome(ID:disease_node_17100) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chromosome 1Q21.1 Deletion Syndrome(ID:disease_node_17105) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chromosome 16P12.1 Deletion Syndrome(ID:disease_node_17110) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chromosome 13Q14 Deletion Syndrome(ID:disease_node_17115) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chromosome 16P12.2-P11.2 Deletion Syndrome(ID:disease_node_17109) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chromosome 1Q41-Q42 Deletion Syndrome(ID:disease_node_17025) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chromosome 15Q25 Deletion Syndrome(ID:disease_node_17112) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chromosome 16P11.2 Deletion Syndrome, 593-Kb(ID:disease_node_17148) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chromosome 17Q23.1-Q23.2 Deletion Syndrome(ID:disease_node_17106) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chromosome 5Q12 Deletion Syndrome(ID:disease_node_17101) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chromosome 16Q22 Deletion Syndrome(ID:disease_node_17108) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chromosome 17Q12 Deletion Syndrome(ID:disease_node_17107) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Chromosomal Disease(ID:disease_node_17149) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chromosome Xp21 Deletion Syndrome(ID:disease_node_17096) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chromosome 4Q21 Deletion Syndrome(ID:disease_node_17102) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chromosome 15Q11.2 Deletion Syndrome(ID:disease_node_17113) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chromosome 16P11.2 Deletion Syndrome, 220-Kb(ID:disease_node_17111) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chromosome 8Q21.11 Deletion Syndrome(ID:disease_node_17098) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chromosome 2P12-P11.2 Deletion Syndrome(ID:disease_node_17104) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chromosome 19P13.13 Deletion Syndrome(ID:disease_node_17097) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chromosome 14Q11-Q22 Deletion Syndrome(ID:disease_node_17114) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Axenfeld-Rieger Syndrome Type 2(ID:disease_node_17085) (Disease) - Incoming r'ship
SUBCLASS_OFto/from 46,Xy Sex Reversal 10(ID:disease_node_15240) (Disease) - Incoming r'ship
SUBCLASS_OFto/from 3P Deletion Syndrome(ID:disease_node_17103) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Alpha Thalassemia-Intellectual Disability Syndrome Type 1(ID:disease_node_15241) (Disease)