neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 1
MONDO:8000012Mondo
Findings
No curated finding names neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 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
- Congenital onset · Infantile onset
HPO, annotations 2026-09-02
Features
59 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.
- AtaxiaHPOHP:0001251
- 2 of 2 reported patients
- Very frequent (80% to 99% of cases)
- BrachycephalyHPOHP:0000248
- 2 of 2 reported patients
- Frequent (30% to 79% of cases)
- Cerebellar atrophyHPOHP:0001272
- 2 of 2 reported patients
- Demyelinating peripheral neuropathyHPOHP:0007108
- 2 of 2 reported patients
- Distal muscle weaknessHPOHP:0002460
- 2 of 2 reported patients
- Frequent (30% to 79% of cases)
- DysmetriaHPOHP:0001310
- 1 of 1 reported patient
- Frequent (30% to 79% of cases)
- Exocrine pancreatic insufficiencyHPOHP:0001738
- 2 of 2 reported patients
- Very frequent (80% to 99% of cases)
- ExotropiaHPOHP:0000577
- 2 of 2 reported patients
- Frequent (30% to 79% of cases)
- Failure to thriveHPOHP:0001508
- 2 of 2 reported patients
- Frequent (30% to 79% of cases)
- Global developmental delayHPOHP:0001263
- 2 of 2 reported patients
- Very frequent (80% to 99% of cases)
- Hepatic fibrosisHPOHP:0001395
- 2 of 2 reported patients
- Hepatic steatosisHPOHP:0001397
- 2 of 2 reported patients
Show the remaining 47
- HypertelorismHPOHP:0000316
- 2 of 2 reported patients
- Occasional (5% to 29% of cases)
- HypothyroidismHPOHP:0000821
- 2 of 2 reported patients
- Occasional (5% to 29% of cases)
- Midface retrusionHPOHP:0011800
- 2 of 2 reported patients
- Moderate intellectual disabilityHPOHP:0002342
- 2 of 2 reported patients
- Very frequent (80% to 99% of cases)
- Motor delayHPOHP:0001270
- 2 of 2 reported patients
- Very frequent (80% to 99% of cases)
- Myopathic faciesHPOHP:0002058
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.
- PTRH2HGNC:24265
- Definitive · G2P · Autosomal recessive · 2020
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2023
- Strong · PanelApp Australia · Autosomal recessive · 2025
Where it sits
Other names
2 names
Resolves to: neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 1
- Also called
- IMNEPDinfantile-onset multisystem neurologic, endocrine, and pancreatic disease