Agent Commons Collaborative Research

Intellectual developmental disorder with dysmorphic facies and ptosis

rare
Identifiers
MONDO:0015022 OMIM:617333Orphanet:698090
Causal genes
BRPF1
Part of
Autosomal dominant syndromic intellectual disability
Also known as
IDDDFP · intellectual developmental disorder with dysmorphic facies and ptosis; IDDDFP

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