paternal 14q32.2 hypomethylation syndrome
MONDO:0016782Mondo
Findings
No curated finding names paternal 14q32.2 hypomethylation syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Features
28 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.
- Delayed speech and language developmentHPOHP:0000750
- Very frequent (80% to 99% of cases)
- HypotoniaHPOHP:0001252
- Very frequent (80% to 99% of cases)
- Intrauterine growth retardationHPOHP:0001511
- Very frequent (80% to 99% of cases)
- Joint hypermobilityHPOHP:0001382
- Very frequent (80% to 99% of cases)
- Motor delayHPOHP:0001270
- Very frequent (80% to 99% of cases)
- Short footHPOHP:0001773
- Very frequent (80% to 99% of cases)
- Small handHPOHP:0200055
- Very frequent (80% to 99% of cases)
- Feeding difficultiesHPOHP:0011968
- Frequent (30% to 79% of cases)
- ObesityHPOHP:0001513
- Frequent (30% to 79% of cases)
- Postnatal growth retardationHPOHP:0008897
- Frequent (30% to 79% of cases)
- Precocious pubertyHPOHP:0000826
- Frequent (30% to 79% of cases)
- Prominent foreheadHPOHP:0011220
- Frequent (30% to 79% of cases)
Show the remaining 16
- Autistic behaviorHPOHP:0000729
- Occasional (5% to 29% of cases)
- ClinodactylyHPOHP:0030084
- Occasional (5% to 29% of cases)
- Decreased facial expressionHPOHP:0004673
- Occasional (5% to 29% of cases)
- Floppy infantHPOHP:0008947
- Occasional (5% to 29% of cases)
- High palateHPOHP:0000218
- Occasional (5% to 29% of cases)
- HypercholesterolemiaHPOHP:0003124
- Occasional (5% to 29% of cases)