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Diseases
Genes (1267)
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MMUT
Methylmalonic Aciduria Due To Methylmalonyl-Coa Mutase Deficiency
LMNA
Mandibuloacral Dysplasia
SSX1
Synovial Sarcoma
SSX2
Synovial Sarcoma
KRT17
Pachyonychia Congenita
RHBDF2
Howel–evans Syndrome
KRT5
Reticular Pigmented Anomaly Of The Flexures
RSPH1
Ciliary Dyskinesia, Primary, 24
POFUT1
Reticular Pigmented Anomaly Of The Flexures
SS18
Synovial Sarcoma
POGLUT1
Reticular Pigmented Anomaly Of The Flexures
KRT16
Pachyonychia Congenita
SERPINB8
Ichthyosis Bullosa Of Siemens
PSENEN
Reticular Pigmented Anomaly Of The Flexures
BCL2
Synovial Sarcoma
Selenium Deficiency
ACE
Severe Acute Respiratory Syndrome
Synovial Sarcoma
Selenium Deficiency
COMT
Neurosis
Reticular Pigmented Anomaly Of The Flexures
Selenium Deficiency
Cognitive Deficit
KRT6A
Pachyonychia Congenita
PSEN1
Cognitive Deficit
MAPT
Cognitive Deficit