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Diseases
Genes (534)
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FGFR2
Pfeiffer Syndrome
Acrocephalosyndactylia
FGFR1
Pfeiffer Syndrome
MEGF8
Carpenter Syndrome 1
RAB23
Carpenter Syndrome 1
PAH
Phenylketonuria (Pku)
FLVCR2
Fowler's Syndrome
IFIH1
Singleton Merten Syndrome
TWIST1
Pfeiffer Syndrome
Acrocephalosyndactylia
CD55
Protein Losing Enteropathy
RB1
Pinealoblastoma
Trilateral Retinoblastoma
VEGFA
Corneal Neovascularization
STAT6
Hemangiopericytoma
FGF2
Pfeiffer Syndrome
Corneal Neovascularization
NAB2
Hemangiopericytoma
IL6
Fibrous Dysplasia Of Bone
Toxoplasmosis
Corneal Neovascularization
Aseptic Meningitis
QDPR
Phenylketonuria (Pku)
ALB
Phenylketonuria (Pku)
Corneal Neovascularization
Protein Losing Enteropathy
Aseptic Meningitis
DDX58
Singleton Merten Syndrome
FLT1
Corneal Neovascularization
PTEN
Thrombophlebitis
Protein Losing Enteropathy
Salmonella Infection