rs864309487
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Patellar aplasia
|
A |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309487
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
EAR, PATELLA, SHORT STATURE SYNDROME
|
A |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309487
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Frontal bossing
|
A |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309487
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Pediatric failure to thrive
|
A |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309487
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Shawl scrotum
|
A |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309487
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Small anterior fontanelle
|
A |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309487
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Mild global developmental delay
|
A |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309487
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Micrognathism
|
A |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309487
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Simple syndactyly of toes, first web space
|
A |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309487
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Delayed bone age
|
A |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309487
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Severe postnatal growth retardation
|
A |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309487
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Intrauterine retardation
|
A |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309487
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Microstomia
|
A |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309487
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Long eyelashes
|
A |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309487
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Stenosis of external auditory canal
|
A |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309487
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Thick vermilion border
|
A |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309488
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Patellar aplasia
|
G |
0.700 |
GeneticVariation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309488
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Depressed nasal bridge
|
G |
0.700 |
GeneticVariation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309488
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Severe postnatal growth retardation
|
G |
0.700 |
GeneticVariation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309488
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Nasogastric tube feeding in infancy
|
G |
0.700 |
GeneticVariation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309488
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Lumbar hyperlordosis
|
G |
0.700 |
GeneticVariation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309488
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Uranostaphyloschisis
|
G |
0.700 |
GeneticVariation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309488
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Mild global developmental delay
|
G |
0.700 |
GeneticVariation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309488
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
EAR, PATELLA, SHORT STATURE SYNDROME
|
G |
0.700 |
GeneticVariation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309488
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Hip Dysplasia
|
G |
0.700 |
GeneticVariation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |