chromosomal deletion syndrome

Term ID

DOID:0060388

Synonyms

Definition

A chromosomal disease that has_material_basis_in partial deletion of chromosomes. (4)

References

Ontology

Human Disease ( DOID:0060388 )

Relationships

is a type of: chromosomal disease

chromosomal disease Show first 5 Terms
has subtype: 3p deletion syndrome 46,XY sex reversal 4 46,XY sex reversal 10 alpha thalassemia-intellectual disability syndrome type 1 AMME complex ... Show All 67 Terms

3p deletion syndrome 46,XY sex reversal 4 46,XY sex reversal 10 alpha thalassemia-intellectual disability syndrome type 1 AMME complex Axenfeld-Rieger syndrome type 2 chromosome 1p36 deletion syndrome chromosome 1q21.1 deletion syndrome 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 chromosome 4q21 deletion syndrome chromosome 5q deletion syndrome 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 chromosome 15q13.3 microdeletion syndrome chromosome 15q24 deletion syndrome chromosome 15q25 deletion syndrome chromosome 15q26-qter deletion syndrome chromosome 16p11.2 deletion syndrome, 220-kb chromosome 16p11.2 deletion syndrome, 593-kb chromosome 16p12.1 deletion syndrome 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 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 distal 10q deletion syndrome hereditary nonpolyposis colorectal cancer type 8 hypoparathyroidism-deafness-renal disease syndrome hypotonia-cystinuria syndrome Jacobsen Syndrome Kleefstra syndrome 1 NFIA-related disorder Phelan-McDermid syndrome posterior amorphous corneal dystrophy Potocki-Shaffer syndrome Rubinstein-Taybi syndrome SATB2-associated syndrome Smith-Magenis syndrome thrombocytopenia-absent radius syndrome velocardiofacial syndrome WAGR syndrome Williams-Beuren syndrome Wolf-Hirschhorn syndrome Y-linked spermatogenic failure 1 Show first 5 Terms

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Alliance (1)

Genes Involved

Zebrafish Models