Also known as: ASCT1 deficiency, SPATCCM, spastic quadriplegia-thin corpus callosum-progressive postnatal microcephaly syndrome, spastic tetraplegia, thin corpus callosum, and progressive microcephaly, spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome
Also known as: SPAHGC, childhood-onset spasticity with hyperglycinemia, childhood-onset spasticity with variant non-ketotic hyperglycinemia, spasticity, childhood-onset, with hyperglycinemia
Also known as: SGD, lactoferrin-deficient neutrophils, neutrophil lactoferrin deficiency, neutrophil-specific granule deficiency, recurrent infection due to specific granule deficiency, specific granule deficiency
Also known as: CEBPE specific granule deficiency, SGD1, lactoferrin-deficient neutrophils, neutrophil lactoferrin deficiency, specific granule deficiency, specific granule deficiency 1, specific granule deficiency caused by mutation in CEBPE
Also known as: SGD2, specific granule deficiency 2
Also known as: dysphasia, specific language disorder
Also known as: specific learning difficulty, specific learning disorder
Also known as: spermatocytic seminoma, spermatocytoma, testicular spermatocytic seminoma
Also known as: SPGF5, infertility associated with multi-tailed spermatozoa and excessive DNA, infertility associated with multitailed spermatozoa and excessive DNA, macrocephalic sperm head syndrome, macrozoospermia, male infertility due to large-headed multiflagellar polyploid spermatozoa, male infertility due to macrozoospermia, male infertility with large-headed, multiflagellar, polyploid spermatozoa, spermatogenic failure 5, spermatogenic failure type 5
Also known as: SPGFY1, Sertoli cell-only syndrome, Y-linked, Sertoli cell-only syndrome, type 1, Sertoli cell-only syndrome, type 2, hypospermatogenesis, incomplete Sertoli cell-only syndrome, spermatogenic failure, Y-linked, 1, spermatogenic failure, Y-linked, 1, Y-linked, spermatogenic failure, Y-linked, type 1
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