The Arc
About The Arc
The Arc is the largest organization in the United States that is solely devoted to improving the lives of all children and adults with cognitive, intellectual and developmental disabilities. The organization offers support to families affected by these diabilities and fosters research and educational programs on the prevention of mental retardation. The Arc is committed to securing opportunities for all people with intellectual and developmental disabilities. To this end, the organization emphasizes personal opportunities for choice in education, housing, employment, and entertainment. The Arc is further committed to reducing the incidence and limiting the consequences of disabilities through research, advocacy, and mutual support. It provides a wide variety of educational materials for parents, teachers, healthcare professionals, and others. Many materials are available in Spanish, and most are free downloads online at www.thearc.org.
Related Rare Diseases:
- Phelan-McDermid Syndrome
- MEF2C Deficiency
- Cerebral Folate Deficiency
- Apert Syndrome
- ADNP Syndrome
- COL4A1/A2-Related Disorders
- SETBP1 Haploinsufficiency Disorder
- KAT6A Syndrome
- Pitt-Hopkins Syndrome
- NGLY1 Deficiency
- Succinic Semialdehyde Dehydrogenase Deficiency
- Fountain Syndrome
- Tay Sachs Disease
- Classic Infantile CLN1 Disease
- Warburg Micro Syndrome
- KCNK9 Imprinting Syndrome
- Cohen Syndrome
- Myhre Syndrome
- Sepiapterin Reductase Deficiency
- ATR-16 Syndrome
- MECP2 Duplication Syndrome
- Congenital Generalized Lipodystrophy
- Congenital Disorders of Glycosylation
- Sporadic Porencephaly
- Brain Small Vessel Disease 1 With or Without Ocular Anomalies
- Lysosomal Free Sialic Acid Storage Disorders
- Wolman Disease
- Triosephosphate Isomerase Deficiency
- Alpha Thalassemia X-linked Intellectual Disability Syndrome
- Megalencephaly-Capillary Malformation
- Lysosomal Storage Disorders
- Megalocornea Intellectual Disability Syndrome
- Fucosidosis
- Costello Syndrome
- MCT8-Specific Thyroid Hormone Cell Transporter Deficiency
- Turner-Type X-Linked Syndromic Intellectual Developmental Disorder
- Laband Syndrome
- Nance-Horan Syndrome
- Trisomy 9p (Multiple Variants)
- KBG Syndrome
- Schindler disease
- Alternating Hemiplegia of Childhood
- Bannayan-Riley-Ruvalcaba Syndrome
- Cutis Marmorata Telangiectatica Congenita
- Mosaic Trisomy 22
- Filippi Syndrome
- Ring Chromosome 4
- Hypomelanosis of Ito
- Smith-Magenis Syndrome
- Schinzel Giedion Syndrome
- Chromosome 15 Ring
- Chromosome 18q- Syndrome
- Chromosome 18 Ring
- Chromosome 9 Ring
- Fetal Hydantoin Syndrome
- Chromosome 22 Ring
- Chromosome 6 Ring
- Kabuki Syndrome
- Cardiofaciocutaneous Syndrome
- Dyggve Melchior Clausen syndrome
- Marinesco-Sjögren Syndrome
- Börjeson-Forssman-Lehman Syndrome
- Penta X Syndrome
- Carpenter Syndrome
- Fragile X Syndrome
- X-linked Opitz G/BBB Syndrome
- Hyperprolinemia Type II
- Sjögren-Larsson Syndrome
- CHARGE Syndrome
- Meningitis
- Oral-Facial-Digital Syndrome
- Isolated Aniridia
- Glutathione Synthetase Deficiency
- AIDS Dysmorphic Syndrome
- Pallister Killian Mosaic Syndrome
- Cerebrocostomandibular Syndrome
- Optic Nerve Hypoplasia
- Seckel Syndrome
- Homocystinuria due to Cystathionine Beta-Synthase Deficiency
- Rubinstein-Taybi Syndrome
- Tetrahydrobiopterin Deficiency
- Coffin Lowry Syndrome
- Alpha-Mannosidosis
- Rasmussen Encephalitis
- Pyruvate Dehydrogenase Complex Deficiency
- Angelman Syndrome
- Leigh Syndrome
- Leprechaunism
- Leukodystrophy
- Russell-Silver Syndrome
- Hydranencephaly
- Zellweger Spectrum Disorders
- Agenesis of Corpus Callosum
- Hartnup Disease
- Fetal Alcohol Syndrome
- Xeroderma Pigmentosum
- Saethre Chotzen Syndrome
- Arginase-1 Deficiency
- Sturge Weber Syndrome
- I Cell Disease
- Pseudo Hurler Polydystrophy
- Sialidosis
- Williams Syndrome
- Smith-Lemli-Opitz Syndrome
- Mucopolysaccharidosis Type III
- Mucopolysaccharidosis Type I
- Rubella
- Sotos Syndrome
- Toxoplasmosis
- Juvenile CLN3 Disease
- Lesch Nyhan Syndrome
- Retinopathy of Prematurity
- Trisomy 13 Syndrome
- Dubowitz Syndrome
- Rett Syndrome
- Pantothenate Kinase-Associated Neurodegeneration
- Coffin-Siris Syndrome
- Carnosinemia
- Froelich Syndrome
- Aicardi Syndrome
- Tuberous Sclerosis
- Cornelia de Lange Syndrome
- Joubert Syndrome
- Cri du Chat Syndrome
- Hydrocephalus
- KAT6B-Related Disorders
- Síndrome de Angelman
- Síndrome de anomalías congénitas múltiples asociado al gen KAT6B
- Trastornos congénitos de la glicosilación (2021)
- Síndrome de Phelan-McDermid
- Sindrome de Sotos
- Síndrome de alfa talasemia-discapacidad intelectual ligada al cromosoma X
- Síndrome de Russell-Silver
- Síndrome de Kabuki
- Esclerosis tuberosa
- Encefalitis de Rasmussen
- Deficiencia de Arginasa-1
- Síndrome de Cohen
- Leucodistrofia
- Froelich Syndrome
- Trisomía 22 en mosaico
- Deficiencia de tetrahidrobiopterina
- Síndrome KAT6A
- Deficiencia del transportador de células de hormona tiroidea específica de MCT8
- Síndrome de Coffin Siris
- Síndrome de Williams
- Síndrome de Opitz G/BBB ligado al cromosoma X
- Lipodistrofia generalizada congénita
- Enfermedad de Tay Sachs
- Deficiencia de NGLY1
- Síndrome orofaciodigital
- Microsíndrome de Warburg
- Síndrome de Smith-Lemli-Opitz
- Imagawa-Matsumoto Syndrome
- Pentasomía X
- Síndrome de Apert
- Síndrome del cromosoma 22q en anillo
- Trastorno del desarrollo intelectual sindrómico ligado al cromosoma X tipo Turner
- Mucopolisacaridosis tipo III
- Síndrome de Imagawa-Matsumoto
- Síndrome de megalencefalia-malformación capilar
- DNM1-Related Epilepsy and Neurodevelopmental Disorder
- TRPM3-Related Neurodevelopmental Disorder
- GM3 Synthase Deficiency
