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Diseases
Genes (529)
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RET
Multiple Endocrine Neoplasia Type 2
Central Hypoventilation Syndrome, Congenital
Phenylketonuria (Pku)
LCAT
Fish-Eye Disease
ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
SCN5A
Cardiac Conduction Defect
WNT5A
Ror2-Related Robinow Syndrome
ANKRD26
Thrombocytopenia 2
PAH
Phenylketonuria (Pku)
PQBP1
Renpenning's Syndrome
FLVCR2
Fowler's Syndrome
IFIH1
Singleton Merten Syndrome
PHOX2B
Pinealoblastoma
Central Hypoventilation Syndrome, Congenital
DVL3
Ror2-Related Robinow Syndrome
DVL1
Ror2-Related Robinow Syndrome
ASCL1
Central Hypoventilation Syndrome, Congenital
FZD2
Ror2-Related Robinow Syndrome
RB1
Pinealoblastoma
Trilateral Retinoblastoma
IL6
Asthma, Nasal Polyps, And Aspirin Intolerance
Argininosuccinic Aciduria
Toxoplasmosis
Aseptic Meningitis
Irritant Contact Dermatitis
Familial Isolated Vitamin E Deficiency
STAT6
Hemangiopericytoma