Any Meckel syndrome in which the cause of the disease is a mutation in the CC2D2A gene.
Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
Acropectorovertebral dysplasia
MONDO:0007058
laurin-Sandrow syndrome
MONDO:0007615
Pallister-Hall syndrome
MONDO:0007804
LADD syndrome
MONDO:0007872
polydactyly of a biphalangeal thumb
MONDO:0008269
polydactyly of an index finger
MONDO:0008271