FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term chromosomal deletion syndrome ID (Ontology) DOID:0060388 (Human Disease)
Definition A chromosomal disease that has_material_basis_in partial deletion of chromosomes.
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
Records annotated with this exact term (annotations to child terms are NOT included)
Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       1
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Alleles Genes
 chromosomal deletion syndrome       1      1
 model of | chromosomal deletion syndrome       1       --
Spanning Tree (Parents/Children)
Only view relationship:
  genetic disease
   |__chromosomal disease
       |__chromosomal deletion syndrome  140 rec.
           |__3p deletion syndrome
           |__46,XY sex reversal 4
           |__46,XY sex reversal 10 1 rec.
           |__alpha thalassemia-intellectual disability syndrome type 1
           |__AMME complex
           |__Axenfeld-Rieger syndrome type 2
           |__chromosome 1p36 deletion syndrome
           |__chromosome 1q21.1 deletion syndrome 4 rec.
           |__chromosome 1q41-q42 deletion syndrome
           |__chromosome 2p12-p11.2 deletion syndrome
           |__chromosome 2p16.1-p15 deletion syndrome
           |__chromosome 2q31.2 deletion syndrome
           |__chromosome 2q37 deletion syndrome
           |__chromosome 3q13.31 deletion syndrome
           |__chromosome 3q29 microdeletion syndrome 13 rec.
           |__chromosome 4q21 deletion syndrome
           |__chromosome 5q deletion syndrome 2 rec.
           |__chromosome 5q12 deletion syndrome
           |__chromosome 6pter-p24 deletion syndrome
           |__chromosome 6q11-q14 deletion syndrome
           |__chromosome 6q24-q25 deletion syndrome
           |__chromosome 8q21.11 deletion syndrome
           |__chromosome 9p deletion syndrome
           |__chromosome 10q23 deletion syndrome
           |__chromosome 13q14 deletion syndrome
           |__chromosome 14q11-q22 deletion syndrome
           |__chromosome 15q11.2 deletion syndrome 12 rec.
           |__chromosome 15q13.3 microdeletion syndrome 2 rec.
           |__chromosome 15q24 deletion syndrome 1 rec.
           |__chromosome 15q25 deletion syndrome
           |__chromosome 15q26-qter deletion syndrome
           |__chromosome 16p11.2 deletion syndrome, 220-kb 2 rec.
           |__chromosome 16p11.2 deletion syndrome, 593-kb 47 rec.
           |__chromosome 16p12.1 deletion syndrome 6 rec.
           |__chromosome 16p12.2-p11.2 deletion syndrome
           |__chromosome 16q22 deletion syndrome
           |__chromosome 17p13.1 deletion syndrome
           |__chromosome 17q11.2 deletion syndrome
           |__chromosome 17q12 deletion syndrome 6 rec.
           |__chromosome 17q23.1-q23.2 deletion syndrome
           |__chromosome 18p deletion syndrome
           |__chromosome 18q deletion syndrome
           |__chromosome 19p13.13 deletion syndrome
           |__chromosome 19q13.11 deletion syndrome
           |__chromosome 22q11.2 deletion syndrome, distal
           |__chromosome Xp21 deletion syndrome
           |__Cri-Du-Chat syndrome
           |__DiGeorge syndrome 8 rec.
           |__distal 10q deletion syndrome
           |__hereditary nonpolyposis colorectal cancer type 8
           |__hypoparathyroidism-deafness-renal disease syndrome 2 rec.
           |__hypotonia-cystinuria syndrome
           |__Jacobsen Syndrome 3 rec.
           |__Kleefstra syndrome 1 4 rec.
           |__NFIA-related disorder 4 rec.
           |__Phelan-McDermid syndrome 1 rec.
           |__posterior amorphous corneal dystrophy
           |__Potocki-Shaffer syndrome
           |__Rubinstein-Taybi syndrome 4 rec.
           |__SATB2-associated syndrome 8 rec.
           |__Smith-Magenis syndrome 1 rec.
           |__thrombocytopenia-absent radius syndrome 1 rec.
           |__velocardiofacial syndrome 1 rec.
           |__WAGR syndrome
           |__Williams-Beuren syndrome 4 rec.
           |__Wolf-Hirschhorn syndrome 2 rec.
           |__Y-linked spermatogenic failure 1
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a chromosomal disease
Part of
hide Synonyms & Secondary IDs
Synonyms
Secondary IDs
hide External Crossreferences & Linkouts