Meier-Gorlin syndrome 9
MONDO:0980992Mondo
Findings
No curated finding names Meier-Gorlin syndrome 9 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
HPO, annotations 2026-09-02
Features
52 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.
- AtelectasisHPOHP:0100750
- 1 of 1 reported patient
- Bulbous noseHPOHP:0000414
- 1 of 1 reported patient
- CardiomegalyHPOHP:0001640
- 1 of 1 reported patient
- CryptorchidismHPOHP:0000028
- 3 of 3 reported patients
- Decreased total lymphocyte countHPOHP:0001888
- 1 of 1 reported patient
- Delayed cranial suture closureHPOHP:0000270
- 1 of 1 reported patient
- Delayed eruption of teethHPOHP:0000684
- 1 of 1 reported patient
- Feeding difficultiesHPOHP:0011968
- 1 of 1 reported patient
- Hyperconvex nailHPOHP:0001795
- 1 of 1 reported patient
- Joint hypermobilityHPOHP:0001382
- 1 of 1 reported patient
- Long noseHPOHP:0003189
- 1 of 1 reported patient
- Low-set earsHPOHP:0000369
- 1 of 1 reported patient
Show the remaining 40
- Metaphyseal irregularityHPOHP:0003025
- 1 of 1 reported patient
- MicrotiaHPOHP:0008551
- 8 of 8 reported patients
- Mild intellectual disabilityHPOHP:0001256
- 2 of 2 reported patients
- Pectus excavatumHPOHP:0000767
- 1 of 1 reported patient
- Posteriorly rotated earsHPOHP:0000358
- 7 of 7 reported patients
- Primary microcephalyHPOHP:0011451
- 1 of 1 reported patient
Where it sits
- A kind of
Other names
2 names
Resolves to: Meier-Gorlin syndrome 9
- Also called
- GINS3 Meier-Gorlin syndromeMGORS9