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ORPHA:300298

Severe congenital hypochromic anemia with ringed sideroblasts

high confidenceDisorder

Also known as: Severe congenital hypochromic sideroblastic anemia

Publications

2

1.9th percentile

Trials

0

Interventional, condition-specific

Researchers

25

Distinct authors in sample

Gene link

STEAP3

Moderate

Readiness

3/6

Stages with a signal

Clinical definition (Orphanet)

A very rare severe non-syndromic hypochromic anemia characterized by transfusion-dependent hypochromic, poorly regenerative anemia and iron overload, resembling non-syndromic sideroblastic anemia except for increased erythrocyte protoporphyrin levels.

How rare: <1 / 1 000 000 — fewer than one in a million. In a city the size of Kolkata, that might mean on the order of fifteen people.

Orphanet entry

Cross-references

Joined from Mondo / Orphanet. MeSH labels may enter searches; UMLS / OMIM / NCIT are stored for reference.

Additional Mondo synonyms (3)

anemia, hypochromic microcytic, with iron overload type 2 · severe congenital hypochromic sideroblastic anaemia · severe congenital hypochromic sideroblastic anemia

Research stages

Trial readiness signals

Where this condition sits on an open-data research pipeline — not how close a treatment is, and not medical advice. Empty stages often mean “not in these databases under this Mondo ID,” not “impossible.”

3/6 stages with a signal

No specific-condition interventional trial, but broader-category trials exist — discuss eligibility with a clinician.

  1. Gene identifiedPresent

    Moderate — STEAP3

  2. LiteraturePresent

    2 matched papers (0 in last 10 years) Source

  3. Phenotype characterisedNot checked

    Not yet enriched from Monarch / HPO

  4. Animal modelNot checked

    Not yet enriched from Monarch / Alliance

  5. Orphan designationNot checked

    FDA/EMA orphan-drug designation not enriched yet

  6. Interventional trialPartial

    None under the specific name; 2114 for broader category anemia

Biology

Genes and phenotypes

Gene–disease validity from GenCC, plus phenotypes and animal models joined from Monarch Initiative via Mondo ID — not a clinical diagnosis aid.

Do we know what causes it?

Probably — there is moderate evidence for STEAP3.

GenCC classification: Moderate.

Phenotypes (Monarch / HPO)

Not enriched in this build — Monarch phenotype joins were not run for this record.

Animal models (Monarch / Alliance)

Not enriched in this build.

Literature

Is anyone studying this?

2

2 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=5449) is 41.

2 papers since the earliest indexed year in this search — median last-10-year count for a rare disease in this dataset is 41 (publications denominator n=5449).

0 in the last 10 years · high confidence · 1.9th percentile (publications denominator)

Phrase hits: 2 · MeSH hits: 0

Open Europe PMC search

Who's working on it?

25

Distinct author names in 2 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
    Baños R1 paper · 2013
    Papers in Europe PMC
  2. 02
    Benítez J1 paper · 2013
    Papers in Europe PMC
  3. 03
    Bogliolo M1 paper · 2013

    Genome Instability and DNA Repair Group, Department of Genetics and Microbiology, Universitat Autònoma de Barcelona, Bellaterra, 08193 Barcelona, Spain.

    Papers in Europe PMC
  4. 04
    Bueren JA1 paper · 2013
    Papers in Europe PMC
  5. 05
    Casado JA1 paper · 2013
    Papers in Europe PMC
  6. 06
    de Winter JP1 paper · 2013
    Papers in Europe PMC
  7. 07
    Derkunt B1 paper · 2013
    Papers in Europe PMC
  8. 08
    GU LIANQUAN1 paper · 2005
    Papers in Europe PMC
  9. 09
    HUANG SHILIANG1 paper · 2005
    Papers in Europe PMC
  10. 10
    HUANG ZHISHU1 paper · 2005
    Papers in Europe PMC

Clinical research

Is a treatment being tested?

0

interventional trials for this specific condition

No interventional trial testing a treatment matched this specific condition name. 1 observational study did — shown below because natural-history and cohort work can be an important step toward a trial. 2,114 trials are registered for anemia, the broader category — shown separately because they may or may not enrol this specific subtype.

Data as of 27 July 2026

No matched interventional trials. This is true for 73% of diseases in the trials denominator (5114 of 7003). Here are the researchers publishing on it.

high confidence · 36.5th percentile (trials denominator)

Recruiting interventional trials

From the matched ClinicalTrials.gov set

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

2,114 interventional trials matched anemia, the broader category — listed below. Those studies are not counted in the condition-specific total.

Broader category: anemia

2,114

Interventional trials for the parent category, exclusive of NCT IDs already counted above. Eligibility for this subtype is not guaranteed.

Worth raising with a clinician. How we count trials.

Recruiting under the broader category

Observational and natural-history studies

1 observational study matches this condition. These do not test a treatment and are not counted in the interventional-trial headline, but they are genuine research: natural-history work often defines the endpoints needed for a future rare-disease trial, and families may be able to enroll.

Recruiting or not-yet-recruiting

Open the complete matched search on ClinicalTrials.gov

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 on the overview but are not added to the query string.

"Severe congenital hypochromic anemia with ringed sideroblasts" OR "Severe congenital hypochromic sideroblastic anemia" OR "anemia, hypochromic microcytic, with iron overload type 2" OR "severe congenital hypochromic sideroblastic anaemia"

Run this search on Europe PMC

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

"Severe congenital hypochromic anemia with ringed sideroblasts" OR "Severe congenital hypochromic sideroblastic anemia" OR "anemia, hypochromic microcytic, with iron overload type 2" OR "severe congenital hypochromic sideroblastic anaemia" OR "STEAP3" OR "anemia, hypochromic microcytic with iron overload" OR "congenital anemia" OR "hereditary anemia"

Recall-expansion terms: STEAP3, anemia, hypochromic microcytic with iron overload, congenital anemia, hereditary anemia

Study-type breakdown: 0 interventional · 1 observational · 0 expanded access. Only interventional studies enter the trial headline.

Parent-category trials query:

"anemia"

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

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

Ingested 2026-07-27T12:38:48.558Z