Clinical beta notice

Disclaimer: These workbenches are the work of a single person, Dr. Ali Al-Ibrahim, they are all in beta and might have errors. Please report bugs, errors and improvements to Alioud16@gmail.com.

Decision-support only — a differential diagnosis, not a diagnosis. Runs entirely in your browser; no patient-identifiable data leaves the device.

Load a demo case

Add phenotype (HPO)

Search by term, synonym or HP:ID.

Selected features (0)

Present 0

Absent 0

Uncertain 0

No phenotypes added yet.

Clinical context (informs inheritance)

Consanguinity Affected sibling(s)

Fetal sex:

Candidate gene(s) — optional (GenCC)

Enter phenotype features and compute to see the ranked differential.

Workbench Reference & About

Version: 1.0b

Guideline version: HPO / GenCC

Last reviewed date: 2026

Formula source: Phenomize Bayesian Engine

Coefficient source: N/A

Validation notes: N/A

Known limitations: N/A

What changed in this version: Initial release.