intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency
Findings
No curated finding names intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency 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
- Adult onset · Infantile onset · Juvenile onset · Neonatal onset · Childhood onset
HPO, annotations 2026-09-02
Features
26 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.
- Bilateral cryptorchidismHPOHP:0008689
- 7 of 7 reported patients
- Decreased body weightHPOHP:0004325
- 12 of 12 reported patients
- Intrauterine growth retardationHPOHP:0001511
- 15 of 15 reported patients
- MicrocephalyHPOHP:0000252
- 10 of 10 reported patients
- Severe short statureHPOHP:0003510
- 12 of 12 reported patients
- Congenital adrenal hypoplasiaHPOHP:0008244
- 12 of 15 reported patients
- HypospadiasHPOHP:0000047
- 5 of 7 reported patients
- Recurrent infectionsHPOHP:0002719
- 10 of 15 reported patients
- Cafe-au-lait spotHPOHP:0000957
- 5 of 15 reported patients
- Decreased response to growth hormone stimulation testHPOHP:0000824
- 5 of 15 reported patients
- OsteopeniaHPOHP:0000938
- 4 of 15 reported patients
- Eczematoid dermatitisHPOHP:0000964
- 3 of 15 reported patients
Show the remaining 14
- ScoliosisHPOHP:0002650
- 3 of 15 reported patients
- SeizureHPOHP:0001250
- 3 of 15 reported patients
- Broad neckHPOHP:0000475
- 1 of 15 reported patients
- ClinodactylyHPOHP:0030084
- 1 of 15 reported patients
- Hodgkin lymphomaHPOHP:0012189
- 1 of 15 reported patients
- LivedoHPOHP:0033832
- 1 of 15 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.
- POLEHGNC:9177
- Strong · G2P · Autosomal recessive · 2023
- Strong · PanelApp Australia · Autosomal dominant · 2025
Where it sits
Other names
1 name
Resolves to: intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency
- Also called
- IMAGE-I syndrome