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Diseases
Genes (515)
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TNNI2
Sheldon-Hall Syndrome
SLC2A10
Hiatal Hernia
Arterial Tortuosity Syndrome
ABCC9
Cantú Syndrome
MYH3
Sheldon-Hall Syndrome
KCNJ8
Cantú Syndrome
LIPA
Acid Lipase Disease
KCNJ11
Diabetes Mellitus, Permanent Neonatal
TPM2
Sheldon-Hall Syndrome
CD55
Protein Losing Enteropathy
TNNT3
Sheldon-Hall Syndrome
PTEN
Intussusception
Social (Pragmatic) Communication Disorder
Thrombophlebitis
Protein Losing Enteropathy
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MEN1
Gastrinoma
ABCC8
Diabetes Mellitus, Permanent Neonatal
GABRA5
Social (Pragmatic) Communication Disorder
SPG29
Spastic Paraplegia 29, Autosomal Dominant
COL1A1
Fibrous Dysplasia Of Bone
Hiatal Hernia
Hernia
THAS
Hernia
C9
Favre–racouchot Syndrome
PIEZO2
Sheldon-Hall Syndrome