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Metadata
ID
SO:0000159
Name
deletion
Parent Relationships
is_a
biological_region
is_a
sequence_alteration
Related Diseases
has material basis in
Kleefstra syndrome 1
chromosomal deletion syndrome
NFIA-related disorder
SATB2-associated syndrome
posterior amorphous corneal dystrophy
hypotonia-cystinuria syndrome
Y-linked spermatogenic failure 1
hereditary nonpolyposis colorectal cancer type 8
alpha thalassemia-intellectual disability syndrome type 1
Axenfeld-Rieger syndrome type 2
Potocki-Shaffer syndrome
46,XY sex reversal 4
46,XY sex reversal 10
AMME complex
DiGeorge syndrome
Cri-Du-Chat syndrome
Williams-Beuren syndrome
Rubinstein-Taybi syndrome
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