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Gene BrowserrightADAM22

ADAM22

ADAM metallopeptidase domain 22

HCNC Approved Symbol
ADAM22 (HGNC:201)
Genomic Coordinates
7:87,934,251 - 88,202,889 (7q21.12)
Synonyms
MDC2
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

Total 1 patient was diagnosed with a variant in the ADAM22 gene.

Frequently observed phenotypes (Top 5 only)

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

01
Patient count
Arthrogryposis multiplex congenita
 1(100.0%)
Patient Count: 1 (100.0%)

% of total patients presenting each phenotype is shown in parentheses.

 1(100.0%)
Clenched hands
 1(100.0%)
Patient Count: 1 (100.0%)

% of total patients presenting each phenotype is shown in parentheses.

 1(100.0%)
Congenital heart defect
 1(100.0%)
Patient Count: 1 (100.0%)

% of total patients presenting each phenotype is shown in parentheses.

 1(100.0%)
Esophageal atresia
 1(100.0%)
Patient Count: 1 (100.0%)

% of total patients presenting each phenotype is shown in parentheses.

 1(100.0%)
Hyperextensible joints
 1(100.0%)
Patient Count: 1 (100.0%)

% of total patients presenting each phenotype is shown in parentheses.

 1(100.0%)
No Results
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Your variant of interest may already be in ClinVar.