CUI Disease Vocabulary Name in Vocabulary Code
C0035934 Rubinstein-Taybi Syndrome DO Holt-Oram syndrome 0060468
C0035934 Rubinstein-Taybi Syndrome DO microphthalmia with limb anomalies 0060861
C0035934 Rubinstein-Taybi Syndrome DO split hand-foot malformation 1 with sensorineural hearing loss 0090024
C0035934 Rubinstein-Taybi Syndrome DO VACTERL association 14679
C0035934 Rubinstein-Taybi Syndrome DO thrombocytopenia-absent radius syndrome 14699
C0035934 Rubinstein-Taybi Syndrome DO Rubinstein-Taybi syndrome 1933
C0035934 Rubinstein-Taybi Syndrome DO Klippel-Trenaunay syndrome 2926
C0035934 Rubinstein-Taybi Syndrome DO nail-patella syndrome 9467
C0035934 Rubinstein-Taybi Syndrome ICD10CM Klippel-Trenaunay-Weber syndrome Q87.2
C0035934 Rubinstein-Taybi Syndrome ICD10CM Nail patella syndrome Q87.2
C0035934 Rubinstein-Taybi Syndrome ICD10CM Rubinstein-Taybi syndrome Q87.2
C0035934 Rubinstein-Taybi Syndrome ICD10CM Thrombocytopenia with absent radius [TAR] syndrome Q87.2
C0035934 Rubinstein-Taybi Syndrome ICD10CM VATER syndrome Q87.2
C0035934 Rubinstein-Taybi Syndrome ICD10CM Holt-Oram syndrome Q87.2
C0035934 Rubinstein-Taybi Syndrome ICD10CM Congenital malformation syndromes predom involving limbs Q87.2
C0035934 Rubinstein-Taybi Syndrome ICD10CM Congenital malformation syndromes predominantly involving limbs Q87.2
C0035934 Rubinstein-Taybi Syndrome ICD10CM Sirenomelia syndrome Q87.2
C0035934 Rubinstein-Taybi Syndrome MONDO Rubinstein-Taybi syndrome due to CREBBP mutations 0008393
C0035934 Rubinstein-Taybi Syndrome MONDO microphthalmia with limb anomalies 0008800
C0035934 Rubinstein-Taybi Syndrome MONDO split hand-foot malformation 1 with sensorineural hearing loss 0009080
C0035934 Rubinstein-Taybi Syndrome MONDO Rubinstein-Taybi syndrome 0019188
C0035934 Rubinstein-Taybi Syndrome MSH Rubinstein-Taybi Syndrome D012415
C0035934 Rubinstein-Taybi Syndrome NCI Rubinstein-Taybi Syndrome C75466
C0035934 Rubinstein-Taybi Syndrome OMIM BROAD THUMB-HALLUX SYNDROME 180849
C0035934 Rubinstein-Taybi Syndrome OMIM RUBINSTEIN-TAYBI SYNDROME 1 180849