fanconi anemia, complementation group 10
MONDO:0979241Mondo
Findings
No curated finding names fanconi anemia, complementation group 10 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
- Congenital onset · Second trimester onset
HPO, annotations 2026-09-02
Features
67 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.
- 2-3 toe cutaneous syndactylyHPOHP:0005709
- 2 of 2 reported patients
- Absent thumbHPOHP:0009777
- 3 of 3 reported patients
- AnemiaHPOHP:0001903
- 1 of 1 reported patient
- BradycardiaHPOHP:0001662
- 1 of 1 reported patient
- Cellular hypersensitivity to mitomycin CHPOHP:0032188
- 1 of 1 reported patient
- Clinodactyly of the 5th fingerHPOHP:0004209
- 2 of 2 reported patients
- CryptorchidismHPOHP:0000028
- 2 of 2 reported patients
- Decreased total leukocyte countHPOHP:0001882
- 1 of 1 reported patient
- Decreased total neutrophil countHPOHP:0001875
- 1 of 1 reported patient
- Duodenal atresiaHPOHP:0002247
- 1 of 1 reported patient
- Failure to thriveHPOHP:0001508
- 1 of 1 reported patient
- HypopituitarismHPOHP:0040075
- 1 of 1 reported patient
Show the remaining 55
- HypotoniaHPOHP:0001252
- 2 of 2 reported patients
- Increased mean corpuscular volumeHPOHP:0005518
- 1 of 1 reported patient
- Increased RBC distribution widthHPOHP:0031965
- 1 of 1 reported patient
- Intrauterine growth retardationHPOHP:0001511
- 1 of 1 reported patient
- OligodactylyHPOHP:0012165
- 1 of 1 reported patient
- PancytopeniaHPOHP:0001876
- 1 of 1 reported patient
Where it sits
- A kind of