RARE DISEASERESEARCH ATLAS

ORPHA:141261

Tessier number 5 facial cleft

high confidence

Query health: suspect — Only one of 2 strategies returned hits (phrase).

Clinical definition (Orphanet)

A rare oblique facial cleft characterized by a unilateral or bilateral defect beginning in the upper lip medial to the oral commissure and extending across the cheek as a groove ending between the middle and lateral third of the lower eyelid (resulting in coloboma). Bone involvement includes an alveolar cleft in the premolar region, extending across the maxilla lateral to the infraorbital nerve and up to the infraorbital rim and orbital floor. The may be associated with Tessier number 3 and number 4 clefts, macrostomia, or anophthalmos.

Orphanet entry

Is anyone studying this?

3

3 papers have ever been indexed under this name. For scale, breast cancer has over 700,000. Median papers in the last 10 years for a rare disease in this dataset (publications denominator n=183) is 38.

3 papers since the earliest indexed year in this search — median last-10-year count for a rare disease in this dataset is 38 (publications denominator n=183).

1 in the last 10 years · high confidence · 9.6th percentile (publications denominator)

Is a treatment being tested?

0

trials for this specific condition

No interventional trial testing a treatment matched this specific condition name on ClinicalTrials.gov (observational studies and pan-disease registries are listed separately when present).

Data as of 26 July 2026

0

no matched trials for facial cleft, the broader category this belongs to either

Parent-category matching found a broader label but no interventional trials under it. How we count trials.

No matched interventional trials. This is true for 59.2% of diseases in the trials denominator (151 of 255). Here are the researchers publishing on it.

high confidence · 29.6th percentile (trials denominator)

Do we know what causes it?

Not yet — the cause hasn't been pinned down in GenCC.

No strong gene–disease assertion joined for this Orphanet entity.

Who's working on it?

19

Distinct author names in 3 sampled papers — named people below.

Who's working on it?

No interventional trial matched this name; these authors publish on it in the sampled literature — a practical starting point for contact.

  1. 01
    Afifi AM1 paper · 2011

    Department of Plastic Surgery, Cleveland Clinic, Cleveland, Ohio

    Papers in Europe PMC
  2. 02
    Alonso N1 paper · 2009
    Papers in Europe PMC
  3. 03
    Brooks S1 paper · 2011

    Department of Plastic Surgery, Cleveland Clinic, Cleveland, Ohio

    Papers in Europe PMC
  4. 04
    Budihardja AS1 paper · 2020

    Department of Oral and Maxillofacial Surgery, Siloam Hospital Lippo Village, University of Pelita Harapan, Jakarta, Indonesia.

    Papers in Europe PMC
  5. 05
    Busato L1 paper · 2009
    Papers in Europe PMC
  6. 06
    Connolly J1 paper · 2011

    Department of Plastic Surgery, Cleveland Clinic, Cleveland, Ohio

    Papers in Europe PMC
  7. 07
    da Silva Freitas R1 paper · 2009

    Federal University of Parana, Grandar, Brazil.

    Papers in Europe PMC
  8. 08
    Dall'Oglio Tolazzi AR1 paper · 2009
    Papers in Europe PMC
  9. 09
    de Oliveria e Cruz GA1 paper · 2009
    Papers in Europe PMC
  10. 10
    Djohan R1 paper · 2011

    Department of Plastic Surgery, Cleveland Clinic, Cleveland, Ohio

    Papers in Europe PMC

Recruiting interventional trials

Trials testing a treatment from the matched ClinicalTrials.gov set

No interventional trial testing a treatment was found for this specific condition name on ClinicalTrials.gov.

Broader category facial cleft also has no matched interventional trial. See who's working on it above — people publishing on this disease are often the practical next contact when no trial is listed.

Where to find support

We do not yet link condition-specific patient organisations. These umbrella groups support undiagnosed and ultra-rare families:

India — NPRD

Last verified 2026-07-26

This ORPHAcode is not on our curated NPRD list (direct or Mondo-parent match). That does not decide clinical eligibility; families in India should ask a notified Centre of Excellence about current coverage.

Hand-curated for this project. ORPHAcode mappings are best-effort and may be incomplete or imprecise for umbrella categories. Parent (Mondo) matches mean the policy lists a broader category — confirm eligibility with a Centre of Excellence. Financial entitlements summarised from public policy statements and may change. This is not official government guidance.

How we counted this

Europe PMC query (preferred label + any corrected label + Orphanet and Mondo exact synonyms, stoplisted; unioned with resolved MeSH labels when available). UMLS / OMIM / NCIT cross-references are stored below but are not added to the query string.

"Tessier number 5 facial cleft"

Run this search on Europe PMC

ClinicalTrials.gov query (quoted phrases + MeSH via query.cond, plus recall-expansion terms when used):

"Tessier number 5 facial cleft" OR "disorder of facial skeleton"

Study-type breakdown: 0 interventional · 0 observational · 0 expanded access. Only interventional studies enter the trial headline.

Cross-references (from Mondo): UMLS:C0432119

Query health: suspect — strategies attempted: phrase, recall-expansion; with hits: phrase

Run this search on ClinicalTrials.gov

Confidence reasoning

  • Preferred label is multi-word and distinctive
  • No synonyms dropped by stoplist
  • No label/synonym collisions with other diseases in this corpus

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