Additional Disease Briefs
Also known as:
DCMD, Mddc, autosomal dominant cystoid macular edema, autosomal dominant cystoid macular oedema, cystoid macular dystrophy, familial macular edema, familial macular oedema, macular dystrophy, dominant cystoid, macular edema, cystoid
Also known as:
CMV retinitis, Cytomegaloviral Retinitis, Cytomegalovirus caused retinitis, Cytomegalovirus retinitis, Retinitis, Cytomegaloviral, cytomegalovirus retinitisCMV retinitis, Cytomegaloviral Retinitis, Cytomegalovirus caused retinitis, Cytomegalovirus retinitis, Retinitis, Cytomegaloviral, cytomegalovirus retinitis
Also known as:
CHP, Winkelmann cytophagic panniculitis
Also known as:
GASTROINTESTINAL ULCERATION, RECURRENT, WITH DYSFUNCTIONAL PLATELETS, GURDP, PLA2G4A-related platelet dysfunction, Phospholipase A2, Group Iva, Deficiency of, cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder, platelet dysfunction due to cytosolic phospholipase-A2 alpha deficiency
Also known as:
Czech dysplasia, Czech dysplasia metatarsal type, Czech dysplasia, metatarsal type, pseudorheumatoid dysplasia progressive, with hypoplastic toes, pseudorheumatoid dysplasia, progressive, with hypoplastic toes, spondyloepiphyseal dysplasia with precocious osteoarthritis
Also known as:
split hand urinary anomalies spina bifida, split hand with obstructive uropathy, spina bifida and diaphragmatic defects, split hand-urinary anomalies-spina bifida syndrome, split-hand with obstructive uropathy, spina bifida, and diaphragmatic defects
Also known as:
D-2-HGA, D-2-hydroxyglutaric acidemia, D-2-hydroxyglutaric aciduria 1, D-2-hydroxyglutaric aciduria type 1, D2HA, D2HGA
Also known as:
17-beta-hydroxysteroid dehydrogenase 4 deficiency, 17-beta-hydroxysteroid dehydrogenase IV deficiency, D-bifunctional enzyme deficiency, DBP deficiency, HSD17B4 deficiency, Pbfe deficiency, bifunctional enzyme deficiency, d-bifunctional protein deficiency, multifunctional enzyme deficiency, peroxisomal bifunctional enzyme deficiency, peroxisomal multifunctional enzyme (MFE2) deficiency, peroxisomal multifunctional enzyme deficiency, pseudo-Zellweger syndrome
Also known as:
D,L-2-HGA, D,L-2-hydroxyglutaric acidemia, D,L-2-hydroxyglutaric aciduria, D2L2AD, combined D-2- and L-2-hydroxyglutaric aciduria, combined D-2-hydroxyglutaric acidemia and L-2-hydroxyglutaric acidemia, combined D-2-hydroxyglutaric aciduria and L-2-hydroxyglutaric aciduria