Seckel syndrome 1

MONDO:0008869

Any Seckel syndrome in which the cause of the disease is a mutation in the ATR gene.

Also known as: ATR Seckel syndrome, SCKL1, Seckel syndrome 1, Seckel syndrome 3, Seckel syndrome caused by mutation in ATR, Seckel syndrome type 1, Bird-headed dwarfism, Sckl

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Broader categories

Disease (679) Hereditary disease (176) Syndromic disease (25) Human disease (14) Autosomal recessive disease (4) Disease of genetic or genomic mechanism (2) Autosomal genetic disease (0) Disease by body system or component (0) Disease by etiologic mechanism (0) Seckel syndrome (0)

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