primordial dwarfism-immunodeficiency-lipodystrophy syndrome
MONDO:0859276Mondo
Findings
No curated finding names primordial dwarfism-immunodeficiency-lipodystrophy syndrome 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
- Fetal onset
HPO, annotations 2026-09-02
Features
56 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.
- Absence of subcutaneous fatHPOHP:0007485
- 5 of 5 reported patients
- BlepharophimosisHPOHP:0000581
- 5 of 5 reported patients
- Decreased circulating IgG concentrationHPOHP:0004315
- 5 of 5 reported patients
- Feeding difficultiesHPOHP:0011968
- 5 of 5 reported patients
- Intrauterine growth retardationHPOHP:0001511
- 5 of 5 reported patients
- Low-set earsHPOHP:0000369
- 5 of 5 reported patients
- MicrocephalyHPOHP:0000252
- 5 of 5 reported patients
- MicrophthalmiaHPOHP:0000568
- 5 of 5 reported patients
- MicrotiaHPOHP:0008551
- 5 of 5 reported patients
- Recurrent infectionsHPOHP:0002719
- 5 of 5 reported patients
- Severe postnatal growth retardationHPOHP:0008850
- 5 of 5 reported patients
- Small handHPOHP:0200055
- 5 of 5 reported patients
Show the remaining 44
- Tapered fingerHPOHP:0001182
- 5 of 5 reported patients
- Decreased total lymphocyte countHPOHP:0001888
- 4 of 5 reported patients
- Severe global developmental delayHPOHP:0011344
- 4 of 5 reported patients
- ThrombocytopeniaHPOHP:0001873
- 4 of 5 reported patients
- HypothyroidismHPOHP:0000821
- 3 of 4 reported patients
- CryptorchidismHPOHP:0000028
- 2 of 3 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.
- PRIM1HGNC:9369
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Strong · G2P · Autosomal recessive · 2025
- Moderate · ClinGen · Autosomal recessive · 2025
- Limited · Ambry Genetics · Autosomal recessive · 2022
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2022
Where it sits
- A kind of