lymphatic malformation 12
MONDO:0031043Mondo
Findings
No curated finding names lymphatic malformation 12 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 · Neonatal death · Death in adolescence · Third trimester onset · Second trimester onset
HPO, annotations 2026-09-02
Features
13 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.
- Fetal ascitesHPOHP:0001791
- 5 of 5 reported patients
- Fetal chylothoraxHPOHP:0025677
- 6 of 6 reported patients
- Fetal pleural effusionHPOHP:0025676
- 7 of 7 reported patients
- LymphedemaHPOHP:0001004
- 7 of 7 reported patients
- Nonimmune hydrops fetalisHPOHP:0001790
- 5 of 7 reported patients
- Hydrocele testisHPOHP:0000034
- 3 of 5 reported patients
- Neonatal respiratory distressHPOHP:0002643
- 4 of 7 reported patients
- Pleural thickeningHPOHP:0031944
- 1 of 2 reported patients
- Fetal pericardial effusionHPOHP:0025671
- 2 of 5 reported patients
- Inguinal herniaHPOHP:0000023
- 2 of 5 reported patients
- PolyhydramniosHPOHP:0001561
- 2 of 5 reported patients
- HyperkeratosisHPOHP:0000962
- 1 of 5 reported patients
Show the remaining 1
- Recurrent upper and lower respiratory tract infectionsHPOHP:0200117
- 1 of 5 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.
- MDFICHGNC:28870
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2022
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Moderate · Ambry Genetics · Autosomal recessive · 2022
Where it sits
- A kind of
Other names
2 names
Resolves to: lymphatic malformation 12
- Also called
- central conducting lymphatic anomalyLMPHM12