STAD syndrome
MONDO:0980973Mondo
Findings
No curated finding names STAD syndrome 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
145 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.
- Accelerated skeletal maturationHPOHP:0005616
- 2 of 2 reported patients
- Agenesis of premolarHPOHP:0011051
- 1 of 1 reported patient
- Amelogenesis imperfectaHPOHP:0000705
- 3 of 3 reported patients
- Aortic regurgitationHPOHP:0001659
- 1 of 1 reported patient
- Aplasia cutis congenita over the scalp vertexHPOHP:0004471
- 1 of 1 reported patient
- Ascending tubular aorta aneurysmHPOHP:0004970
- 1 of 1 reported patient
- Atopic dermatitisHPOHP:0001047
- 1 of 1 reported patient
- Atrial septal defectHPOHP:0001631
- 1 of 1 reported patient
- BrachydactylyHPOHP:0001156
- 1 of 1 reported patient
- Cerebellar dysplasiaHPOHP:0007033
- 1 of 1 reported patient
- Cerebellar hypoplasiaHPOHP:0001321
- 1 of 1 reported patient
- Cleft palateHPOHP:0000175
- 2 of 2 reported patients
Show the remaining 133
- CNS demyelinationHPOHP:0007305
- 1 of 1 reported patient
- Cone-shaped epiphysisHPOHP:0010579
- 4 of 4 reported patients
- Curly hairHPOHP:0002212
- 2 of 2 reported patients
- Cutis laxaHPOHP:0000973
- 1 of 1 reported patient
- Cutis marmorataHPOHP:0000965
- 1 of 1 reported patient
- Decreased circulating insulin-like growth factor 1 concentrationHPOHP:0030353
- 1 of 1 reported patient
Where it sits
- A kind of