Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome
MONDO:0014689Mondo
Findings
No curated finding names Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
HPO, annotations 2026-09-02
Features
19 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.
- Bulbous noseHPOHP:0000414
- 2 of 2 reported patients
- Cervical C2/C3 vertebral fusionHPOHP:0004602
- 2 of 2 reported patients · Congenital onset
- Low posterior hairlineHPOHP:0002162
- 2 of 2 reported patients
- MicrocephalyHPOHP:0000252
- 2 of 2 reported patients
- PtosisHPOHP:0000508
- 2 of 2 reported patients
- Webbed neckHPOHP:0000465
- 2 of 2 reported patients · Congenital onset
- Everted lower lip vermilionHPOHP:0000232
- 1 of 2 reported patients
- Generalized hypotoniaHPOHP:0001290
- 1 of 2 reported patients
- High palateHPOHP:0000218
- 1 of 2 reported patients
- Long philtrumHPOHP:0000343
- 1 of 2 reported patients
- Low-set earsHPOHP:0000369
- 1 of 2 reported patients · Congenital onset
- MicrognathiaHPOHP:0000347
- 1 of 2 reported patients
Show the remaining 7
- Motor delayHPOHP:0001270
- 1 of 2 reported patients
- Narrow foreheadHPOHP:0000341
- 1 of 2 reported patients
- Short statureHPOHP:0004322
- 1 of 2 reported patients
- Thin upper lip vermilionHPOHP:0000219
- 1 of 2 reported patients
- Underdeveloped nasal alaeHPOHP:0000430
- 1 of 2 reported patients
- MyopathyHPOHP:0003198
- Nemaline bodiesHPO
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.
- MYO18BHGNC:18150
- Definitive · ClinGen · Autosomal recessive · 2025
- Definitive · G2P · Autosomal recessive · 2023
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2020
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Moderate · Ambry Genetics · Autosomal recessive · 2020
- Moderate · Ambry Genetics · Autosomal recessive · 2025
- Supportive · Orphanet · Autosomal recessive · 2021