All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05693 brain calcification calcification, brain - - 10 10 JAM2 - -
06531 IBGC8 Basal ganglia calcification, idiopathic, 8, autosomal recessive 618824 AR - - JAM2 - onset adulthood; no microcephaly; no cataracts; no facial dysmorphisms; developmental delay; rare seizures; spasticity; no hypotonia; intracranial calcifications; no intracranial hemorrhage; no ventriculomegaly; no corpus callosum anomalies; no hepatomegaly; no renal anomalies
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