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ABHD5
- Cerebral Creatine Deficiency
MYO5B
- Microvillus Inclusion Disease
GAMT
- Guanidinoacetate Methyltransferase Deficiency
ALS2
- Infantile-Onset Ascending Hereditary Spastic Paralysis
UMOD
- Medullary Cystic Kidney Disease
MC2R
- Familial Glucocorticoid Deficiency
STX3
- Microvillus Inclusion Disease
SRD5A2
- Alopecia, Androgenetic, 1
AR
- Alopecia, Androgenetic, 1
MRAP
- Familial Glucocorticoid Deficiency
WWTR1
- Epithelioid Hemangioendothelioma
CAMTA1
- Epithelioid Hemangioendothelioma
TFE3
- Epithelioid Hemangioendothelioma
VDR
- Alopecia, Androgenetic, 1
- Lumbar Disc Disease
YAP1
- Epithelioid Hemangioendothelioma
CILP
- Lumbar Disc Disease
TNFRSF10A
- Alopecia, Androgenetic, 1
- Lumbar Disc Disease
COL9A3
- Lumbar Disc Disease
ABCC2
- Alopecia, Androgenetic, 1
SUPV3L1
- Alopecia, Androgenetic, 1