rs864309488
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
MEIER-GORLIN SYNDROME 6
|
|
0.800 |
GeneticVariation |
UNIPROT |
|
|
|
rs864309488
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
MEIER-GORLIN SYNDROME 6
|
G |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs864309486
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Congenital small ears
|
T |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309486
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Atresia of the external auditory canal
|
T |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309486
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Micrognathism
|
T |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309486
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Intrauterine retardation
|
T |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309486
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Delayed bone age
|
T |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309486
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Entropion
|
T |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309486
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Hypoplastic female external genitalia
|
T |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309486
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
MEIER-GORLIN SYNDROME 6
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs864309486
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Umbilical hernia
|
T |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309486
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Thick vermilion border
|
T |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309486
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Subglottic stenosis
|
T |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309486
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Tracheomalacia
|
T |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309486
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Prominent forehead
|
T |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309486
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Nasogastric tube feeding in infancy
|
T |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309486
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Severe failure to thrive
|
T |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309486
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Patellar aplasia
|
T |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309486
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Abnormality of the middle phalanx of the 5th finger
|
T |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309486
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Severe postnatal growth retardation
|
T |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309486
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Downward slant of palpebral fissure
|
T |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309486
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
Anteverted nostril
|
T |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |
rs864309486
|
Entrez Id: |
51053 |
Gene Symbol: |
GMNN |
GMNN
|
EAR, PATELLA, SHORT STATURE SYNDROME
|
T |
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
|
Short palpebral fissure
|
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
|
Congenital small ears
|
A |
0.700 |
CausalMutation |
CLINVAR |
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
|
26637980 |
2015 |