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Features include: Diarrhea, Vomiting, Generalized aminoaciduria, and Failure to thrive and 6 more.
Organ System | Phenotype Count | Example Features |
|---|---|---|
Digestive system | 4 | Diarrhea, Vomiting, Abnormal intestine morphology |
Growth and development |
Biomarker and diagnostic research for homozygous 11P15-p14 deletion syndrome has been reported in the published literature.
No clinical trials have been registered for homozygous 11P15-p14 deletion syndrome.
98 publications have been identified in PubMed for homozygous 11P15-p14 deletion syndrome. Research spans Basic Science / Preclinical (49%), Case Report / Case Series (34%), and Epidemiology / Natural History (8%).
Research Type | Count | % of Total |
|---|---|---|
Laboratory research | 48 | 49% |
Data assembled from 4 of 12 sources · Last updated Sep 20, 2026, 8:43 AM UTC
Online Mendelian Inheritance in Man
1
Failure to thrive |
Kidneys and urinary system | 1 | Renal tubular dysfunction |
Ears | 1 | Congenital sensorineural hearing impairment |
Pregnancy and birth | 1 | Congenital sensorineural hearing impairment |
Patient case studies
33 |
34% |
Disease patterns and progression | 8 | 8% |
Testing and diagnosis research | 5 | 5% |
Research summaries | 4 | 4% |
DuBois M (2026). [PMID: 40937658](https://pubmed.ncbi.nlm.nih.gov/40937658/). *American journal of medical genetics. Part A*. [Epidemiology / Natural History]
Palmeri S (2026). [PMID: 41365842](https://pubmed.ncbi.nlm.nih.gov/41365842/). *Rheumatology (Oxford, England)*. [Basic Science / Preclinical]
Kaur N (2026). [PMID: 41689604](https://pubmed.ncbi.nlm.nih.gov/41689604/). *Neurogenetics*. [Case Report / Case Series]
Hiltebeitel LR (2025). [PMID: 39229650](https://pubmed.ncbi.nlm.nih.gov/39229650/). *American journal of medical genetics. Part A*. [Basic Science / Preclinical]
Murgiano L (2025). [PMID: 39971978](https://pubmed.ncbi.nlm.nih.gov/39971978/). *Scientific reports*. [Basic Science / Preclinical]
Essid M (2025). [PMID: 39993789](https://pubmed.ncbi.nlm.nih.gov/39993789/). *Clinical genetics*. [Review / Meta-Analysis]
Cordova Hurtado E (2025). [PMID: 41081394](https://pubmed.ncbi.nlm.nih.gov/41081394/). *Biology open*. [Case Report / Case Series]
Wang Y (2025). [PMID: 40450688](https://pubmed.ncbi.nlm.nih.gov/40450688/). *Cell reports*. [Case Report / Case Series]
Almazán Monroy JD (2025). [PMID: 41025026](https://pubmed.ncbi.nlm.nih.gov/41025026/). *Oxford medical case reports*. [Epidemiology / Natural History]
Wu B (2025). [PMID: 40237971](https://pubmed.ncbi.nlm.nih.gov/40237971/). *Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology*. [Case Report / Case Series]