FG syndrome type 2
FG syndrome type 2
An X-linked condition (OMIM:300321) characterised by mental retardation, relative macrocephaly, hypotonia and constipation.Molecular pathology
Defects in FLNA cause FG syndrome type 2.
Molecular pathology
Defects in FLNA cause FG syndrome type 2.
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- Ffxii
- FFXO
- FFY
- FFY
- FFYA
- FFYB
- FFYC
- FFYDP
- FFYI
- FFyL
- FFYNDP
- FFYP
- FFYR
- FFYS
- FFYSA
- FFZ
- FFZC
- FFZE
- FFZEV
- FFZX
- FG
- FG
- FG
- FG
- FG achromatism
- Fg Off
- FG Sagittae
- FG Syndrome
- FG Syndrome
- FG syndrome 1
- FG syndrome type 2
- FG Universe
- FG&B
- FG-42
- FG-DVC
- FG-LDPC
- FG1
- FG42
- FGA
- FGA
- FGAA
- FGAAR
- FGAC
- FGAE
- FGAF
- FGAG
- FGAM
- FGAMP
- FGAN
- FGAO
- FGAPI
- FGAR
- FGAR
- FGAS
- FGASA
- FGAT
- FGATD
- FGAW
- FGAWR
- FGAY
- FGB
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