toluene embryopathy
Also known as: Hersh Podruch Weisskopk syndrome, microcephaly, central nervous system dysfunction, minor craniofacial and limb anomalies, and variable growth deficiency, toluene embryopathy
Also known as: Hersh Podruch Weisskopk syndrome, microcephaly, central nervous system dysfunction, minor craniofacial and limb anomalies, and variable growth deficiency, toluene embryopathy
Also known as: Primary tonsillar lymphoma, lymphoma of the tonsil, lymphoma of tonsil, tonsil lymphoma, tonsillar lymphoma
Also known as: STHAG4, WNT10A tooth agenesis, lateral incisors, absence of, lateral incisors, pegged or missing, succedaneous teeth, agenesis of, tooth agenesis caused by mutation in WNT10A, tooth agenesis, selective, 4, tooth agenesis, selective, 4, with or without ectodermal dysplasia, tooth agenesis, selective, type 4
Also known as: Toriello-Carey syndrome, agenesis of corpus callosum with facial anomalies and Robin sequence, corpus callosum agenesis facial anomalies Robin sequence, corpus callosum agenesis-blepharophimosis-Robin sequence syndrome, corpus callosum, agenesis of, with facial anomalies and ROBIN sequence
Also known as: Toriello Lacassie Droste syndrome, aplasia cutis congenita with epibulbar dermoids, aplasia cutis congenita-epibulbar dermoids syndrome, oculo-ectodermal syndrome, oculoectodermal syndrome, oculoectodermal syndrome, somatic, oes
Also known as: torsade DE pointes, short-coupled variant
Also known as: DYT13, dystonia 13, torsion, autosomal dominant, primary dystonia with mixed phenotype, primary dystonia, DYT13 type, primary torsion dystonia with predominant craniocervical or upper limb onset, torsion dystonia type 13
Also known as: DYT17, dystonia 17, torsion, autosomal recessive, dystonia-17, primary torsion, primary dystonia, DYT17 type, torsion dystonia type 17
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