bifid nose, autosomal recessive - Symptoms, Causes & Research | Kisho | Kisho

bifid nose, autosomal recessive

Rare Disease

MONDO:0008866

Also known as:

autosomal recessive bifid nosebifid nose, autosomal recessiveNose, Median cleft of

Autosomal recessive form of bifid nose.

Genes

–

Clinical Trials

6 total

Newborn Screening

–

Patient Groups

–

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

How we create this content →

Last reviewed: Feb 2026

Evidence base: Early

Clinical Trials

Research studies investigating treatments and therapies for this condition.

Active Trials

Total Trials

Filter trials on ClinicalTrials.gov:

View All Trials

Data from ClinicalTrials.gov Jan 7, 2026

Clinical Trials

Research studies investigating treatments and therapies for this condition.

Active Trials

Total Trials

Filter trials on ClinicalTrials.gov:

View All Trials

Data from ClinicalTrials.gov Jan 7, 2026

Overview

Limited structured data is available for this condition. Information continues to be gathered as research progresses.(3 data sources · Data coverage: Limited)

Overview

bifid nose, autosomal recessive is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Symptoms & Signs

This condition is characterized as an autosomal recessive form of bifid nose. There are no known associated genes, inheritance patterns, or documented symptoms available in the current data. Additionally, there are no orphan drug designations under investigation.

Prognosis & Outlook

Patients and caregivers are encouraged to seek genetic counseling to understand the implications of this inherited condition. Connecting with rare disease registries such as NORD or Orphanet may provide additional resources and support. Finding specialists experienced with similar conditions can also be beneficial.

Quick Resources

Helpful links for rare disease information and support

GARD (Genetic and Rare Diseases Information Center)NORD (National Organization for Rare Disorders)

General Questions to Consider

Questions that may be helpful when speaking with your healthcare team

•Are there specialists or centers of excellence with experience in this condition?
•Is there a patient registry I could participate in?
•What clinical trials might be available for this condition?
•Are there patient advocacy groups I should connect with?

Clinical

Limited Clinical Data

Clinical profile data for this condition is not yet available. Phenotype information may still be loading below.

Treatment

Clinical Trials

Research studies investigating treatments and therapies for this condition.

Active Trials

Total Trials

Filter trials on ClinicalTrials.gov:

View All Trials

Data from ClinicalTrials.gov Jan 7, 2026

Support

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:210400

GARD

Genetic and Rare Diseases Info Center

GARD:15142

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AI-Generated Content: This summary was generated using AI. Always consult with qualified healthcare providers for medical guidance.

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bifid nose, autosomal recessive

Patient-Friendly Information

Clinical Trials

Clinical Trials

Overview

Overview

Symptoms & Signs

Prognosis & Outlook

Quick Resources

General Questions to Consider

Clinical

Limited Clinical Data

Treatment

Clinical Trials

Support

External Resources

OMIM

GARD

Related Diseases

Know a Patient Advocacy Group for this condition?

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