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Features include sometimes findings: Seizure. 3 total HPO annotations.
Organ System | Phenotype Count | Example Features |
|---|---|---|
Brain and nerves | 2 | Moderate intellectual disability, Seizure |
Biomarker and diagnostic research for intellectual disability, autosomal recessive 10 has been reported in the published literature.
No clinical trials have been registered for intellectual disability, autosomal recessive 10.
57 publications have been identified in PubMed for intellectual disability, autosomal recessive 10. Research spans Case Report / Case Series (38%), Basic Science / Preclinical (21%), and Diagnostic / Biomarker (15%).
Research Type | Count | % of Total |
|---|---|---|
Patient case studies | 20 | 38% |
Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 1:06 PM UTC
Online Mendelian Inheritance in Man
Genetic and Rare Diseases Info Center
Laboratory research
11 |
21% |
Testing and diagnosis research | 8 | 15% |
Research summaries | 7 | 13% |
Disease patterns and progression | 5 | 9% |
Other research | 1 | 2% |
New treatment approaches | 1 | 2% |
Ting SL (2026). [PMID: 41968386](https://pubmed.ncbi.nlm.nih.gov/41968386/). *Am J Med Genet A*. [Diagnostic / Biomarker]
Harripaul R (2026). [PMID: 41865132](https://pubmed.ncbi.nlm.nih.gov/41865132/). *Sci Rep*. [Basic Science / Preclinical]
Ek M (2026). [PMID: 41514368](https://pubmed.ncbi.nlm.nih.gov/41514368/). *Genome medicine*. [Diagnostic / Biomarker]
Alimoradi E (2026). [PMID: 41656075](https://pubmed.ncbi.nlm.nih.gov/41656075/). *Molecular genetics & genomic medicine*. [Case Report / Case Series]
Yigit ZM (2026). [PMID: 40960173](https://pubmed.ncbi.nlm.nih.gov/40960173/). *American journal of medical genetics. Part A*. [Case Report / Case Series]
Manti F (2026). [PMID: 41450729](https://pubmed.ncbi.nlm.nih.gov/41450729/). *Neurology. Genetics*. [Gene Therapy / Novel Therapeutics]
Pan X (2026). [PMID: 41764152](https://pubmed.ncbi.nlm.nih.gov/41764152/). *Journal of molecular medicine (Berlin, Germany)*. [Diagnostic / Biomarker]
Zhu L (2026). [PMID: 41721346](https://pubmed.ncbi.nlm.nih.gov/41721346/). *Orphanet journal of rare diseases*. [Case Report / Case Series]
Kiss S (2026). [PMID: 41631259](https://pubmed.ncbi.nlm.nih.gov/41631259/). *JIMD reports*. [Case Report / Case Series]
Mengistu DY (2026). [PMID: 42063344](https://pubmed.ncbi.nlm.nih.gov/42063344/). *Development*. [Basic Science / Preclinical]