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Diseases
Genes (1016)
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HMBS
Acute Intermittent Porphyria
SH3TC2
Charcot-Marie-Tooth Neuropathy Type 4c
MMUT
Methylmalonic Aciduria Due To Methylmalonyl-Coa Mutase Deficiency
KRT17
Pachyonychia Congenita
RHBDF2
Howel–evans Syndrome
TMEM67
Coach Syndrome
SRY
Xy Gonadal Dysgenesis
Coarctation Of The Aorta
SSX1
Synovial Sarcoma
SSX2
Synovial Sarcoma
RPGRIP1L
Coach Syndrome
CC2D2A
Coach Syndrome
ACE
Severe Acute Respiratory Syndrome
Coarctation Of The Aorta
Synovial Sarcoma
KRT16
Skin Condition
Pachyonychia Congenita
SS18
Synovial Sarcoma
WT1
Xy Gonadal Dysgenesis
Coarctation Of The Aorta
NR5A1
Xy Gonadal Dysgenesis
THPO
Severe Acute Respiratory Syndrome
Thrombocythemia
MPL
Thrombocythemia
JAK2
Thrombocythemia
SOX9
Xy Gonadal Dysgenesis