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TNF
- Neurogenic Inflammation
- Fanconi Anemia, Complementation Group J
- Monoclonal Gammopathy Of Undetermined Significance
TP63
- Acro–dermato–ungual–lacrimal–tooth Syndrome
SLC25A22
- Episodic Ataxia
- Early Myoclonic Encephalopathy
PNKP
- Pes Cavus
- Episodic Ataxia
- Dna Repair-Deficiency Disorder
- Chromosome Instability Syndrome
TBX4
- Ischiopatellar Dysplasia
FLNB
- Atelosteogenesis Type I
MED12
- Lujan–fryns Syndrome
KCTD1
- Scalp–ear–nipple Syndrome
KANSL1
- 17q21.31 Microdeletion Syndrome
FANCC
- Fanconi Anemia, Complementation Group J
FANCG
- Fanconi Anemia, Complementation Group J
BRIP1
- Fanconi Anemia, Complementation Group J
FANCM
- Fanconi Anemia, Complementation Group J
FANCA
- Fanconi Anemia, Complementation Group J
FANCD2
- Fanconi Anemia, Complementation Group J
SLX4
- Fanconi Anemia, Complementation Group J
FANCL
- Fanconi Anemia, Complementation Group J
FLNA
- Melnick–needles Syndrome
POMC
- Cortisone Reductase Deficiency
- Neurogenic Inflammation
- Hypernatremia
WRN
- Fanconi Anemia, Complementation Group J
- Dna Repair-Deficiency Disorder
- Chromosome Instability Syndrome