fibromuscular dysplasia, multifocal
MONDO:0859151Mondo
Findings
No curated finding names fibromuscular dysplasia, multifocal yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
31 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.
- Arterial fibromuscular dysplasiaHPOHP:0005313
- 4 of 4 reported patients
- Vertebral artery tortuosityHPOHP:0033981
- 4 of 4 reported patients
- MigraineHPOHP:0002076
- 5 of 6 reported patients
- Tortuous cerebral arteriesHPOHP:0004938
- 3 of 4 reported patients
- Carotid artery tortuosityHPOHP:0005302
- 2 of 4 reported patients
- Celiac artery dissectionHPOHP:0033982
- 2 of 4 reported patients
- Hyperextensible skinHPOHP:0000974
- 3 of 6 reported patients
- Joint hypermobilityHPOHP:0001382
- 3 of 6 reported patients
- Joint subluxationHPOHP:0032153
- 3 of 6 reported patients
- Narrow noseHPOHP:0000460
- 3 of 6 reported patients
- Atrophic scarsHPOHP:0001075
- 2 of 6 reported patients
- Deeply set eyeHPOHP:0000490
- 2 of 6 reported patients
Show the remaining 19
- DolichocephalyHPOHP:0000268
- 2 of 6 reported patients
- Downslanted palpebral fissuresHPOHP:0000494
- 2 of 6 reported patients
- Pectus excavatumHPOHP:0000767
- 2 of 6 reported patients
- Pes planusHPOHP:0001763
- 2 of 6 reported patients
- Soft skinHPOHP:0000977
- 2 of 6 reported patients
- Soft, doughy skinHPOHP:0001027
- 2 of 6 reported patients
Where it sits
- A kind of