pancytopenia-developmental delay syndrome
MONDO:0014317Mondo
Findings
No curated finding names pancytopenia-developmental delay syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Juvenile onset · Early young adult onset
HPO, annotations 2026-09-02
Features
7 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- AnemiaHPOHP:0001903
- 3 of 3 reported patients
- Bone marrow hypocellularityHPOHP:0005528
- 3 of 3 reported patients
- Decreased total leukocyte countHPOHP:0001882
- 3 of 3 reported patients
- ThrombocytopeniaHPOHP:0001873
- 3 of 3 reported patients
- MicrocephalyHPOHP:0000252
- 2 of 3 reported patients
- Neonatal hypotoniaHPOHP:0001319
- 1 of 3 reported patients
- Cutaneous photosensitivityHPOHP:0000992
- 0 of 3 reported patients
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- ERCC6L2HGNC:26922
- Definitive · Ambry Genetics · Autosomal recessive · 2023
- Definitive · G2P · Autosomal recessive · 2015
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2023
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Supportive · Orphanet · Autosomal recessive · 2021
Where it sits
Other names
2 names
Resolves to: pancytopenia-developmental delay syndrome
- Also called
- bone marrow failure syndrome type 2Trilineage bone marrow failure-developmental delay syndrome