Atelis syndrome 1
MONDO:0859575Mondo
Findings
No curated finding names Atelis syndrome 1 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
- Infantile onset
HPO, annotations 2026-09-02
Features
32 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.
- Global developmental delayHPOHP:0001263
- 7 of 7 reported patients
- Cafe-au-lait spotHPOHP:0000957
- 3 of 7 reported patients
- Feeding difficultiesHPOHP:0011968
- 3 of 7 reported patients
- AnemiaHPOHP:0001903
- 2 of 7 reported patients
- Attention deficit hyperactivity disorderHPOHP:0007018
- 2 of 7 reported patients
- Eczematoid dermatitisHPOHP:0000964
- 2 of 7 reported patients
- HypothyroidismHPOHP:0000821
- 2 of 7 reported patients
- HypotoniaHPOHP:0001252
- 2 of 7 reported patients
- Long faceHPOHP:0000276
- 2 of 7 reported patients
- Recurrent infectionsHPOHP:0002719
- 2 of 7 reported patients
- Atrial septal defectHPOHP:0001631
- 1 of 7 reported patients
- Autistic behaviorHPOHP:0000729
- 1 of 7 reported patients
Show the remaining 20
- Basilar invaginationHPOHP:0012366
- 1 of 7 reported patients
- BronchiectasisHPOHP:0002110
- 1 of 7 reported patients
- Carious teethHPOHP:0000670
- 1 of 7 reported patients
- CataractHPOHP:0000518
- 1 of 7 reported patients
- Decreased anti-CD3/28-induced T-cell proliferationHPOHP:0031382
- 1 of 7 reported patients
- Decreased total leukocyte countHPOHP:0001882
- 1 of 7 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.
- SLF2HGNC:17814
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Moderate · Ambry Genetics · Autosomal recessive · 2023
- Moderate · G2P · Autosomal recessive · 2023