neurocardiorenal malformation syndrome
MONDO:0980704Mondo
Findings
No curated finding names neurocardiorenal malformation 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
- Congenital onset · Fetal onset · Third trimester onset
HPO, annotations 2026-09-02
Features
87 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
- 2-3 toe syndactylyHPOHP:0004691
- 1 of 1 reported patient
- 3-4 finger cutaneous syndactylyHPOHP:0011939
- 1 of 1 reported patient
- Abnormal cortical gyrationHPOHP:0002536
- 2 of 2 reported patients
- Absent speechHPOHP:0001344
- 1 of 1 reported patient
- Aggressive behaviorHPOHP:0000718
- 1 of 1 reported patient
- AlopeciaHPOHP:0001596
- 1 of 1 reported patient
- AsthmaHPOHP:0002099
- 1 of 1 reported patient
- Axial hypotoniaHPOHP:0008936
- 3 of 3 reported patients
- Bilateral cryptorchidismHPOHP:0008689
- 1 of 1 reported patient
- BradycardiaHPOHP:0001662
- 1 of 1 reported patient
- Broad-based gaitHPOHP:0002136
- 1 of 1 reported patient
Show the remaining 75
- BronchitisHPOHP:0012387
- 1 of 1 reported patient
- BruxismHPOHP:0003763
- 2 of 2 reported patients
- Cerebellar vermis hypoplasiaHPOHP:0001320
- 1 of 1 reported patient
- Chronic constipationHPOHP:0012450
- 1 of 1 reported patient
- Chronic rhinitisHPOHP:0002257
- 1 of 1 reported patient
- Convex nasal ridgeHPOHP:0000444
- 1 of 1 reported patient