Additional Disease Briefs

Axenfeld-Rieger syndrome type 3

Also known as: Axenfeld anomaly, Axenfeld-Rieger anomaly, Axenfeld-Rieger anomaly with Cardiac defects and/Or sensorineural hearing loss, Axenfeld-Rieger anomaly with or without Cardiac defects and/or sensorineural hearing loss, Axenfeld-Rieger anomaly with or without cardiac defects and/or sensorineural hearing loss, Axenfeld-Rieger syndrome caused by mutation in FOXC1, Axenfeld-Rieger syndrome type 3, Axenfeld-Rieger syndrome, type 3, FOXC1 Axenfeld-Rieger syndrome, RIEG3, Rieger anomaly, Rieger syndrome type 3, Rieger syndrome, type 3, anterior chamber Cleavage syndrome, anterior chamber cleavage syndrome, anterior segment mesenchymal dysgenesis

axial mesodermal dysplasia spectrum

Also known as: Russell Weaver Bull syndrome, Russell-Weaver-Bull syndrome, blastogenesis defect

axial spondylometaphyseal dysplasia

Also known as: SMDAX, SmD axial, SmD, axial, axial SmD, spondylometaphyseal dysplasia axial type, spondylometaphyseal dysplasia, axial

AXIN2-related attenuated familial adenomatous polyposis

Also known as: AXIN2-related AFAP, AXIN2-related attenuated FAP, AXIN2-related attenuated familial polyposis coli

axonal polyneuropathy associated with IgG/IgM/IgA monoclonal gammopathy

Ayme-Gripp syndrome

Also known as: AYGRP, AYME-Gripp syndrome, Ayme-Gripp syndrome, Aymé-Gripp syndrome, cataracts, congenital, with sensorineural deafness, Down syndrome-like Facial appearance, short stature, and intellectual disability, cataracts, congenital, with sensorineural deafness, Down syndrome-like Facial appearance, short stature, and mental retardation

azygos continuation of the inferior vena cava

Also known as: azygos continuation of the IVC, azygos continuation of the inferior caval vein

B-cell acute lymphoblastic leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)

Also known as: B acute lymphoblastic leukaemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1), B acute lymphoblastic leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1), B lymphoblastic leukaemia lymphoma with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1) (morphologic abnormality), B lymphoblastic leukemia lymphoma with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1) (morphologic abnormality), B-acute lymphoblastic leukaemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1), B-acute lymphoblastic leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1), B-lymphoblastic leukemia/lymphoma with TCF3-PBX1, B-lymphoblastic leukemia/lymphoma with t(1;19)(q23;p13.3)

B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome

Also known as: BILU syndrome, Hoffman syndrome