NDIS Conditions & Diagnoses
Explore NDIS eligibility, funded supports and provider guides for 119 disability conditions and diagnoses across Australia.
- Autism Spectrum Disorder
- Intellectual Disability
- ADHD
- Specific Learning Disability
- Speech & Language Impairment
- Dyslexia
- Down Syndrome (Trisomy 21)
- Fragile X Syndrome
- Angelman Syndrome
- Prader-Willi Syndrome
- Rett Syndrome
- Williams Syndrome
- Tuberous Sclerosis Complex
- Cornelia de Lange Syndrome
- Smith-Magenis Syndrome
- Phelan-McDermid Syndrome
- CHARGE Syndrome
- Cri du Chat Syndrome
- Kabuki Syndrome
- Costello Syndrome
- Klinefelter Syndrome
- Phenylketonuria (PKU)
- Neurofibromatosis
- Acquired Brain Injury
- Cerebral Palsy
- Epilepsy
- Multiple Sclerosis
- Motor Neurone Disease
- Parkinson's Disease
- Huntington's Disease
- Stroke
- Spina Bifida
- Spinal Muscular Atrophy
- Tourette Syndrome
- Joubert Syndrome
- Mitochondrial Disease
- Landau-Kleffner Syndrome
- Alzheimer's Disease
- Duchenne Muscular Dystrophy
- Muscular Dystrophy
- Spinal Cord Injury
- Charcot-Marie-Tooth Disease
- Limb Difference
- Cystic Fibrosis
- Hereditary Spastic Paraplegia
- Ehlers-Danlos Syndrome
- Blindness & Low Vision
- Deafness & Hearing Impairment
- Deafblindness
- Auditory Processing Disorder
- Sensory Processing Disorder
- Schizophrenia
- Schizoaffective Disorder
- Bipolar Disorder
- Major Depression
- Borderline Personality Disorder
- Post-Traumatic Stress Disorder
- Obsessive-Compulsive Disorder
- Anxiety Disorders
- Eating Disorders
- Personality Disorders
- Fibromyalgia
- Myalgic Encephalomyelitis / Chronic Fatigue Syndrome
- Inflammatory Arthritis
- Lupus (SLE)
- Chronic Pain
- Type 1 Diabetes
- Global Developmental Delay
- Developmental Delay (ECEI/under 7)
- Retinitis Pigmentosa
- Usher Syndrome
- Epidermolysis Bullosa
- Hydrocephalus
- Turner Syndrome
- Noonan Syndrome
- Batten Disease (NCL)
- Niemann-Pick Disease
- Wolf-Hirschhorn Syndrome
- Limb Amputation (Acquired)
- 22q11.2 Deletion Syndrome (DiGeorge)
- Achondroplasia (Dwarfism)
- Arthrogryposis
- Bardet-Biedl Syndrome
- CDKL5 Deficiency Disorder
- Cerebral Visual Impairment (CVI)
- Chiari Malformation
- Chronic Kidney Disease (End-Stage Renal)
- Coffin-Siris Syndrome
- Complex Regional Pain Syndrome (CRPS)
- Crohn's Disease & Inflammatory Bowel Disease
- Dissociative Identity Disorder
- Dravet Syndrome
- Dup15q Syndrome
- Dystonia
- Edwards Syndrome (Trisomy 18)
- Foetal Alcohol Spectrum Disorder (FASD)
- FOXG1 Syndrome
- Friedreich's Ataxia
- Guillain-Barré Syndrome & CIDP
- Lennox-Gastaut Syndrome
- Long COVID
- Marfan Syndrome
- Mowat-Wilson Syndrome
- Mucopolysaccharidosis (MPS)
- Multiple System Atrophy (MSA)
- Myasthenia Gravis
- Osteogenesis Imperfecta
- Pitt-Hopkins Syndrome
- Post-Polio Syndrome
- Postural Orthostatic Tachycardia Syndrome (POTS)
- Progressive Supranuclear Palsy (PSP)
- Scleroderma (Systemic Sclerosis)
- Scoliosis (Severe / Neuromuscular)
- Sotos Syndrome
- Spinocerebellar Ataxia
- Sturge-Weber Syndrome
- SYNGAP1-Related Disorder
- Transverse Myelitis
- Younger Onset Dementia