anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism - Symptoms, Causes & Research | Kisho | Kisho

anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism

Rare Disease

MONDO:0008790

Also known as:

Genes

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Clinical Trials

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Newborn Screening

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Patient Groups

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Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Last reviewed: Feb 2026

Evidence base: Early

Limited structured data is available for this condition. Information continues to be gathered as research progresses.(2 data sources · Data coverage: Limited)

Overview

anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Symptoms & Signs

The inheritance pattern for this condition is known to be autosomal recessive. There are currently no orphan drug designations under investigation for this condition.

Prognosis & Outlook

Patients and caregivers are encouraged to seek genetic counseling to understand the implications of the autosomal recessive inheritance. Connecting with rare disease registries and online patient communities may provide additional support and resources.

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?

Limited structured data is available for this condition. Information continues to be gathered as research progresses.(2 data sources · Data coverage: Limited)

Overview

anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Symptoms & Signs

The inheritance pattern for this condition is known to be autosomal recessive. There are currently no orphan drug designations under investigation for this condition.

Prognosis & Outlook

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?

Overview

Limited structured data is available for this condition. Information continues to be gathered as research progresses.(2 data sources · Data coverage: Limited)

Overview

anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Symptoms & Signs

The inheritance pattern for this condition is known to be autosomal recessive. There are currently no orphan drug designations under investigation for this condition.

Prognosis & Outlook

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

Inheritance Pattern

Autosomal Recessive

Inheritance patterns describe how genetic conditions are passed from parents to children.

Treatment

Support

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:206400

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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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anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism

Patient-Friendly Information

Overview

Symptoms & Signs

Prognosis & Outlook

Quick Resources

General Questions to Consider

Overview

Symptoms & Signs

Prognosis & Outlook

Quick Resources

General Questions to Consider

Overview

Overview

Symptoms & Signs

Prognosis & Outlook

Quick Resources

General Questions to Consider

Clinical

Inheritance Pattern

Treatment

Support

External Resources

OMIM

Related Diseases

Know a Patient Advocacy Group for this condition?

Need this data in your product?