Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the ANG gene.
Comprehensive, easy-to-understand information about this condition
How we create this content →Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 6, 2026
Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 6, 2026
The documentation for amyotrophic lateral sclerosis type 9 is limited due to its rarity and the recent identification of its genetic basis. Conditions like ALS9 often affect fewer individuals, which restricts the scope of systematic clinical studies. As research continues, more information about clinical features and management options may become available.
To navigate your care effectively, seek a neurologist with expertise in hereditary motor neuron diseases. Genetic counseling is also recommended to understand the implications of the ANG gene mutation for you and your family. While there are currently no designated patient organizations for ALS9, resources such as the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can provide valuable information. Additionally, consider looking for natural history studies or registries that may arise as research progresses.
Actionable guidance for navigating care for amyotrophic lateral sclerosis type 9
To navigate your care effectively, seek a neurologist with expertise in hereditary motor neuron diseases. Genetic counseling is also recommended to understand the implications of the ANG gene mutation for you and your family. While there are currently no designated patient organizations for ALS9, resources such as the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can provide valuable information. Additionally, consider looking for natural history studies or registries that may arise as research progresses.
Consider asking your healthcare providers these condition-specific questions
Helpful links for rare disease information and support
Inheritance patterns describe how genetic conditions are passed from parents to children.
Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 6, 2026
Consider asking your healthcare providers these condition-specific questions
Online Mendelian Inheritance in Man
Genetic and Rare Diseases Info Center
AI-Generated Content: This summary was generated using AI. Always consult with qualified healthcare providers for medical guidance.
Kisho delivers this disease record via API, including phenotypes (HPO), genes, orphan drug designations, screening status, and PAG mapping, with version history and governance.