intellectual developmental disorder, X-linked, syndromic 37
MONDO:0958322Mondo
Findings
No curated finding names intellectual developmental disorder, X-linked, syndromic 37 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- X-linked inheritance
- Onset and course
- Neonatal onset
HPO, annotations 2026-09-02
Features
199 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.
- Feeding difficultiesHPOHP:0011968
- 5 of 5 reported patients
- HypertrichosisHPOHP:0000998
- 2 of 2 reported patients
- Intellectual disabilityHPOHP:0001249
- 4 of 4 reported patients
- Joint hypermobilityHPOHP:0001382
- 2 of 2 reported patients
- MacrocephalyHPOHP:0000256
- 2 of 2 reported patients
- MyopiaHPOHP:0000545
- 4 of 4 reported patients
- NystagmusHPOHP:0000639
- 1 of 1 reported patient
- ScoliosisHPOHP:0002650
- 4 of 4 reported patients
- SeizureHPOHP:0001250
- 1 of 1 reported patient
- Visual impairmentHPOHP:0000505
- 1 of 1 reported patient
- Delayed fine motor developmentHPOHP:0010862
- 16 of 18 reported patients
- Delayed speech and language developmentHPOHP:0000750
- 16 of 18 reported patients
Show the remaining 187
- Delayed ability to walkHPOHP:0031936
- 15 of 18 reported patients
- HypotoniaHPOHP:0001252
- 13 of 18 reported patients
- Inguinal herniaHPOHP:0000023
- 13 of 18 reported patients
- Thin upper lip vermilionHPOHP:0000219
- 12 of 18 reported patients
- HypospadiasHPOHP:0000047
- 8 of 14 reported patients
- AutismHPOHP:0000717
- 9 of 18 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.
- ZFXHGNC:12869
- Strong · PanelApp Australia · X-linked · 2025
- Limited · Ambry Genetics · X-linked · 2024