GARD Information Navigator | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program

GARD Information Navigator | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program

GARD Information Navigator

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Do you need help finding the information you need? GARD now has an interactive tool to help you quickly find information on our website. For select diseases, the GARD Information Navigator lets you choose the topics you want - like diagnosis, treatment, financial aid, finding a specialist, and more. You'll get a custom results page for each topic you select. This may include related questions and answers posted on the GARD disease pages, links to credible resources, and contact information for advocacy organizations. The results page also includes video tutorials and written guides, developed by GARD, with tips for finding information, resources, and services. These results are hand-picked by GARD Information Specialists with you in mind.

The GARD Information Navigator is currently available for the following diseases, with more added every month.

47 XXX syndrome
Acute intermittent porphyria
Adiposis dolorosa
Adrenomyeloneuropathy
Alopecia universalis
Alpha-1 antitrypsin deficiency
Apert syndrome
Aquagenic pruritus
Arachnoiditis
Arginase deficiency
Arthrogryposis multiplex congenita
Bardet-Biedl syndrome
Bartter syndrome
Becker muscular dystrophy
Bilateral perisylvian polymicrogyria
Bronchiolitis obliterans
Brugada syndrome
Canavan disease
Cat eye syndrome
Cholesteatoma
Chromosome 3p- syndrome
Chronic hiccups
Cleidocranial dysplasia
Coats disease
Cold agglutinin disease
Cold urticaria
Congenital adrenal hyperplasia
Dent disease
Ehlers-Danlos syndromes
Evans syndrome
Factor V deficiency
Factor V Leiden thrombophilia
Familial breast cancer
Familial Mediterranean fever
Fatal familial insomnia
Fetal valproate syndrome
Fragile X syndrome
Friedreich ataxia
Gardner syndrome
Glucose transporter type 1 deficiency syndrome
Glutaric acidemia type I
Goldenhar disease
Hailey-Hailey disease
Hemophagocytic lymphohistiocytosis
Hereditary spherocytosis
Horner's syndrome
Huntington disease
Hypermobile Ehlers-Danlos syndrome
Hypokalemic periodic paralysis
Hypophosphatemic rickets
Joubert syndrome
Juvenile myoclonic epilepsy
Kabuki syndrome
Kartagener syndrome
Kikuchi disease
Klinefelter syndrome
Krabbe disease
Kyphoscoliotic Ehlers-Danlos syndrome
Leigh syndrome
Lewy body dementia
Lichen planus pigmentosus
Liddle syndrome
Linear nevus sebaceous syndrome
Mastocytosis
McCune-Albright syndrome
Ménière's disease
Migraine with brainstem aura
Morphea
MTHFR gene variant
Multicentric Castleman Disease
Multiple familial trichoepithelioma
Multiple myeloma
Myasthenia gravis
Neurofibromatosis type 1
Neuromyelitis optica
Ollier disease
Opitz G/BBB syndrome
Opsoclonus-myoclonus syndrome
Osteomyelitis
Osteopetrosis
Pachyonychia congenita
Parsonage Turner syndrome
Pelizaeus-Merzbacher disease
Postorgasmic illness syndrome
Postural orthostatic tachycardia syndrome
Prader-Willi syndrome
Primary hyperoxaluria type 1
Progressive hemifacial atrophy
Progressive osseous heteroplasia
Progressive supranuclear palsy
Pseudocholinesterase deficiency
Rett syndrome
Russell-Silver syndrome
Schwannoma
Septo-optic dysplasia spectrum
Sjogren syndrome
Sneddon syndrome
Spinal muscular atrophy
Spinal muscular atrophy 1
Spinal muscular atrophy type 2
Spinocerebellar ataxia
Spondylodysplastic Ehlers-Danlos syndrome
Subacute sclerosing panencephalitis
Superior mesenteric artery syndrome
Susac syndrome
Synovial sarcoma
Systemic mastocytosis
Tietze syndrome
Transient global amnesia
Trimethylaminuria
Tubular aggregate myopathy
Turner syndrome
Vascular Ehlers-Danlos syndrome
VLCAD deficiency
Von Hippel-Lindau disease
Wagner syndrome
Williams syndrome
X-linked periventricular heterotopia
Zellweger syndrome