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MYO5B
- Microvillus Inclusion Disease
ALS2
- Infantile-Onset Ascending Hereditary Spastic Paralysis
MC2R
- Familial Glucocorticoid Deficiency
STX3
- Microvillus Inclusion Disease
CD55
- Protein Losing Enteropathy
RB1
- Pinealoblastoma
- Trilateral Retinoblastoma
MRAP
- Familial Glucocorticoid Deficiency
IFNG
- Hepatitis E
- Legionnaires' Disease
- Yellow Fever
- Viral Hemorrhagic Fevers
TLR5
- Legionnaires' Disease
CILP
- Lumbar Disc Disease
STAR
- Adrenal Crisis
- Familial Glucocorticoid Deficiency
COL9A3
- Lumbar Disc Disease
GABRA5
- Social (Pragmatic) Communication Disorder
SART3
- Disseminated Superficial Actinic Porokeratosis
ASPN
- Lumbar Disc Disease
PTEN
- Social (Pragmatic) Communication Disorder
- Thrombophlebitis
- Lumbar Disc Disease
- Protein Losing Enteropathy
COL11A1
- Lumbar Disc Disease
MARK3
- Visual Impairment And Progressive Phthisis Bulbi
TXNRD2
- Familial Glucocorticoid Deficiency
NNT
- Familial Glucocorticoid Deficiency