neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation
MONDO:0032921Mondo
Findings
No curated finding names neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
HPO, annotations 2026-09-02
Features
33 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.
- Absent speechHPOHP:0001344
- 4 of 4 reported patients
- Gastrostomy tube feeding in infancyHPOHP:0011471
- 4 of 4 reported patients
- Hypoplasia of the corpus callosumHPOHP:0002079
- 4 of 4 reported patients
- HypotoniaHPOHP:0001252
- 4 of 4 reported patients
- Motor delayHPOHP:0001270
- 4 of 4 reported patients
- Neonatal respiratory distressHPOHP:0002643
- 4 of 4 reported patients · Neonatal onset
- Poor head controlHPOHP:0002421
- 4 of 4 reported patients · Infantile onset
- Recurrent viral infectionsHPOHP:0004429
- 4 of 4 reported patients
- Severe global developmental delayHPOHP:0011344
- 4 of 4 reported patients
- Infantile spasmsHPOHP:0012469
- 3 of 4 reported patients
- Anteverted naresHPOHP:0000463
- 2 of 4 reported patients
- Cerebral visual impairmentHPOHP:0100704
- 2 of 4 reported patients
Show the remaining 21
- Gingival overgrowthHPOHP:0000212
- 2 of 4 reported patients
- SpasticityHPOHP:0001257
- 2 of 4 reported patients
- Thick eyebrowHPOHP:0000574
- 2 of 4 reported patients
- Vesicoureteral refluxHPOHP:0000076
- 2 of 4 reported patients
- BrachycephalyHPOHP:0000248
- 1 of 4 reported patients
- CataractHPOHP:0000518
- 1 of 4 reported patients · Childhood onset
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.
- RALGAPA1HGNC:17770
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2020
- Strong · G2P · Autosomal recessive · 2020
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Moderate · Ambry Genetics · Autosomal recessive · 2020