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PROS1
- Thrombophilia Due To Protein S Deficiency, Autosomal Dominant
- Protein S Deficiency
- Thrombophilia Due To Protein S Deficiency, Autosomal Recessive
- Urinary Tract Infection (Uti)
TPMT
- Thiopurine S Methyltranferase Deficiency
HBB
- Sickle Cell Disease
PMS2
- Mismatch Repair Cancer Syndrome
MLH1
- Mismatch Repair Cancer Syndrome
MSH6
- Mismatch Repair Cancer Syndrome
MSH2
- Mismatch Repair Cancer Syndrome
TBX4
- Ischiopatellar Dysplasia
ADSL
- Adenylosuccinase Deficiency
AHCY
- Hypermethioninemia With S-Adenosylhomocysteine Hydrolase Deficiency
TREX1
- Retinal Vasculopathy With Cerebral Leukoencephalopathy And Systemic Manifestations
TFG
- Hereditary Motor And Sensory Neuropathy With Proximal Dominance
FAM111B
- Hereditary Fibrosing Poikiloderma With Tendon Contractures, Myopathy, And Pulmonary Fibrosis
FLNA
- Melnick–needles Syndrome
NR2E3
- Enhanced S-Cone Syndrome
POMC
- Urinary Tract Infection (Uti)
- Catalepsy
TNF
- Urinary Tract Infection (Uti)
- Sickle Cell Disease
- Shigellosis
- Tuberculoma
- Rare Form Of Salmonellosis
- Mycoplasma Pneumonia
- Pneumococcal Infection
WDR73
- Galloway Mowat Syndrome
OSGEP
- Galloway Mowat Syndrome
LAGE3
- Galloway Mowat Syndrome