Disease #00101 (AT3D (Antithrombin III deficiency), OMIM:613118)

Official abbreviation AT3D
Name Antithrombin III deficiency
OMIM ID 613118
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene SERPINC1
Associated tissues -
Disease features -
Remarks -


Individuals

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00000558 A T Norlelawati et al.(2014) F Malaysia Malay - - - AT3D - SERPINC1 SERPINC1 1 1 Nur Aisyah Athirah
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