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Summary Literature (0)
MIM:213980 - CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME 1; CFSMR1

Xenbase Genes: tmco1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008952 - obsolete cerebrofaciothoracic dysplasia
MONDO:0800436 - craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1