CEBALID syndrome

MONDO:0032908

Also known as: MCTT, MN1 C-Terminal Truncation Syndrome, MN1 C-terminal truncation syndrome, CEBALID, CEBALID SYNDROME, Craniofacial Defects, Dysmorphic Ears, Structural Brain Abnormalities, Expressive Language Delay, and Impaired Intellectual Development

0 clinical trials for this condition and its sub-types, 0 tagged with CEBALID syndrome itself.

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↑ Hereditary disease (18235)

Including sub-types (0) Tagged with CEBALID syndrome (0)

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