Behind The Mystery Cares For Rare
November 15, 2022
For over a decade, we’ve proudly given a voice to the voiceless in the rare community. Behind the Mystery collaborates with pharmaceutical companies, foundations, and patient advocacy groups to educate the public on rare and genetic diseases through our recurring segment on Lifetime Television.
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22q11.2 deletion syndrome / DiGeorge syndrome
A
Alpha-1 (Understanding Alpha-1)
Alpha-1 (Alpha-1 antitrypsin deficiency or AAT)
Autosomal Dominant Hypocalcemia Type 1 (ADH1)
Autosomal dominant polycystic kidney disease (ADPKD)
B
Blastic plasmacytoid dendritic cell neoplasm (BPDCN)
C
Chronic Thromboembolic Pulmonary Hypertension (CTEPH)
Complex Regional Pain Syndrome
Congenital Sucrase-isomaltase Deficiency
Cystic Fibrosis & Neuromuscular Diseases
D
E
Exocrine Pancreatic Insufficiency
F
Fibrodysplasia Ossificans Progressiva (FOP) 1
Fibrodysplasia Ossificans Progressiva (FOP) 2
G
Generalized myasthenia gravis (gMG)
H
Hereditary Antithrombin (AT) Deficiency
Homozygous Familial Hypercholesterolemia
I
Infantile Severe Malignant Osteopetrosis
L
Lysosomal Acid Lipase (LAL) Deficiency
M
N
Neonatal-Onset Multisystem Inflammatory Disease (NOMID)
Neurogenic orthostatic hypotension [nOH] (1)
Neurogenic orthostatic hypotension [nOH] (2)
Nontuberculous Mycobacteria (NTM)
O
Ornithine transcarbamylase (OTC) deficiency – Urea Cycle Disorder
P
Paroxysmal Nocturnal Hemoglobinuria
Pediatric Growth Hormone Deficiency
Pheochromocytoma and Paragangliona
Polycythemia Vera/Myeloproliferative neoplasms [MPNs] (1)
Polycythemia Vera/Myeloproliferative neoplasms [MPNs] (2)s
Primary hemophgocytic lymphohistiocytosis
Pulmonary Arterial Hypertension
R
S
T
U
V
W
X
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