Airing weekdays at 7:30 A.M. on

Airing weekdays at 7:30 A.M. on

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

Acromegaly

Acute Hepatic Porphria

Al Amyloidosis

Alpha-1 (Understanding Alpha-1)

Alpha-1 (Alpha-1 antitrypsin deficiency or AAT)

Alport Syndrome

Arginase I Deficiency

ATTR Amyloidosis (1)

ATTR Amyloidosis (2)

ATTR Polyneuropahy

Autosomal Dominant Hypocalcemia Type 1 (ADH1)

Autosomal dominant polycystic kidney disease (ADPKD)

B

Blastic plasmacytoid dendritic cell neoplasm (BPDCN)

C

Cancer of Unknown Primary

Castleman’s Disease

Chondrosarcoma

Chronic Granulomatous Disease

Chronic Thromboembolic Pulmonary Hypertension (CTEPH)

Complex Regional Pain Syndrome

Congenital Sucrase-isomaltase Deficiency

Cooley’s Anemia

Cushing syndrome (1)

Cushing syndrome (2)

Cystic Fibrosis & Neuromuscular Diseases

Cystinosis

D

Dravet Syndrome

Duchenne Muscular Dystrophy

E

ENPP1 Deficiency

Epidermolysis Bullosa

Exocrine Pancreatic Insufficiency

F

Fibrodysplasia Ossificans Progressiva (FOP) 1

Fibrodysplasia Ossificans Progressiva (FOP) 2

Fragile X

Friedreich’s Ataxia

G

Generalized myasthenia gravis (gMG)

Glioblastoma (1)

Glioblastoma (2)

H

Hereditary Antithrombin (AT) Deficiency

Hodgkin’s Lymphoma

Homozygous Familial Hypercholesterolemia

Hunter Syndrome

I

Idiopathic Pulmonary Fibrosis

IgA Nephropathy

Infantile onset Pompe Disease

Infantile Severe Malignant Osteopetrosis

Interstitial cystitis

L

Late-onset Pompe Disease

Lennox-Gastaut Syndrome

Lysosomal Acid Lipase (LAL) Deficiency

M

Myelofibrosis

N

Narcolepsy

Neonatal-Onset Multisystem Inflammatory Disease (NOMID)

Neuroendocrine Tumors

Neurogenic orthostatic hypotension [nOH] (1)

Neurogenic orthostatic hypotension [nOH] (2)

Non-24 Hour Disorder

Nontuberculous Mycobacteria (NTM)

NRG-1 Solid Tumors

O

Ornithine transcarbamylase (OTC) deficiency – Urea Cycle Disorder

P

Paroxysmal Nocturnal Hemoglobinuria

Pediatric Growth Hormone Deficiency

Pheochromocytoma and Paragangliona

Plasminogen Deficiency (PLGD)

Polycythemia Vera/Myeloproliferative neoplasms [MPNs] (1)

Polycythemia Vera/Myeloproliferative neoplasms [MPNs] (2)s

Pompe Disease

Primary hemophgocytic lymphohistiocytosis

Primary Periodic Paralysis

Pulmonary Arterial Hypertension

Pulmonary Fibrosis

R

RH Factor

S

Sarcoidosis

Sickle Cell Disease (1)

Sickle Cell Disease (2)

SLE Lupus

Systemic Mastocytosis

T

Tyrosinemia (HT-1)

U

Uveal Melanoma

V

Von Willebrand

W

Wilson Disease

X

X-linked hypophosphatemia (XLT)

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