/Seckel syndrome 5

Seckel syndrome 5

Rare Disease

MONDO:0013443

Also Known As

CEP152 Seckel syndromeSCKL5Seckel syndrome 5Seckel syndrome caused by mutation in CEP152Seckel syndrome type 5

Any Seckel syndrome in which the cause of the disease is a mutation in the CEP152 gene.

Comprehensive, easy-to-understand information about this condition

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Gene data from MyGene.info • Click to view on NCBI Gene

Seckel syndrome 1

MONDO:0008869

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Lowry-Wood syndrome

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Hallermann-Streiff syndrome

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hypoparathyroidism-retardation-dysmorphism syndrome

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microcephalic primordial dwarfism, Toriello type

MONDO:0009616