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Smith-Lemli-Opitz Syndrome

Disease ID: disease_node_9876

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DbxrefGARD:5683, ICD10CM:E78.72, MESH:D019082, MIM:270400, NCI:C85071, SNOMEDCT_US_2023_03_01:43929004, UMLS_CUI:C0175694
SubclassofDOID_3146
Data SourceDOID, MESH
SynonymsRutledge lethal multiple congenital anomaly syndrome, Smith-Opitz-Inborn syndrome
Mesh IdD019082
Mesh LabelSmith-Lemli-Opitz Syndrome
Mesh SubclassofD008052, D000015, D050171, D043202
Doid LabelSmith-Lemli-Opitz syndrome
Doid DescriptionOMIM mapping confirmed by DO. [LS].
Disease Node Iddisease_node_9876
Doid IdDOID_14692
LabelSmith-Lemli-Opitz Syndrome
Doid Alternate IdsDOID_4366