Also known as: SLVL, SMZL, marginal zone lymphoma of spleen, marginal zone lymphoma of the spleen, splenic lymphoma with circulating villous lymphocytes, splenic marginal zone B-cell lymphoma, splenic marginal zone B-cell lymphoma with villous lymphocytes, splenic marginal zone lymphoma, splenic marginal zone lymphoma with villous lymphocytes
Also known as: SGFLD syndrome, Sgfld syndrome, splenogonadal fusion limb defect syndrome, splenogonadal fusion limb defects micrognatia, splenogonadal fusion limb defects syndrome, splenogonadal fusion with limb defects and micrognathia
Also known as: SHFD1, SHFM1, ectrodactyly, split hand-foot malformation type 1, split hand/foot malformation 1, split-hand deformity, split-hand/foot deformity 1, split-hand/foot malformation 1, split-hand/foot malformation 1 with or without deafness, split-hand/foot malformation type 1
Also known as: SHFM1D, congenital deafness with split hands and feet, deafness, congenital, with split hands and feet, split hand-foot malformation 1 with sensorineural hearing loss, split hand-split foot-deafness syndrome, split-hand/foot malformation 1 with sensorineural hearing loss, split-hand/foot malformation 1 with sensorineural hearing loss, autosomal recessive
Also known as: SHFD2, SHFM2, SHSF2, split hand foot anomaly - X-linked, split hand foot deformity 2, split hand-foot malformation type 2, split hand/foot malformation 2, split hand/foot malformation X-linked, split-hand/foot deformity 2, split-hand/foot malformation 2, split-hand/split-foot anomaly, X-linked
Also known as: 10q24 microduplication syndrome, Buttiens Fryns syndrome, Buttiens-Fryns syndrome, SHFM3, Shsf3, chromosome 10Q24 Duplication syndrome, chromosome 10q24 duplication syndrome, distal limb deficiencies with micrognathia, distal limb deficiencies-micrognathia syndrome, limb deficiencies distal with micrognathia, limb deficiencies, distal, with micrognathia, split hand-foot malformation 3, split hand-foot malformation type 3, split-hand/foot malformation 3, split-hand/foot malformation 3, gene duplication syndrome, split-hand/foot malformation type 3
Also known as: SHFM4, TP63 split hand-foot malformation, split hand-foot malformation caused by mutation in TP63, split hand-foot malformation type 4, split-hand/foot malformation 4, split-hand/foot malformation type 4
Also known as: SHFM5, split hand-foot malformation type 5, split-hand/foot malformation 5, split-hand/foot malformation type 5
Also known as: SHFM6, WNT10B split hand-foot malformation, ectrodactyly, autosomal recessive, split hand-foot malformation caused by mutation in WNT10B, split hand-foot malformation type 6, split-hand/foot malformation 6, split-hand/foot malformation type 6
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