SESSILE SERRATED POLYPOSIS CANCER SYNDROME; SSPCS |
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SEVERE CANAVAN DISEASE |
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SEVERE COMBINED IMMUNODEFICIENCY WITH MICROCEPHALY, GROWTH RETARDATION, AND SENSITIVITY TO IONIZING RADIATION |
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SEVERE COMBINED IMMUNODEFICIENCY WITH SENSITIVITY TO IONIZING RADIATION |
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SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY |
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SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CELL-POSITIVE |
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SEVERE CONGENITAL NEMALINE MYOPATHY |
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SEVERE CUTANEOUS ADVERSE REACTION, SUSCEPTIBILITY TO |
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SEVERE EARLY-ONSET OBESITY-INSULIN RESISTANCE SYNDROME DUE TO SH2B1 DEFICIENCY |
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SEVERE HEREDITARY THROMBOPHILIA DUE TO CONGENITAL PROTEIN S DEFICIENCY |
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SÉZARY SYNDROME |
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SHAHEEN SYNDROME; SHNS |
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SHASHI-PENA SYNDROME; SHAPNS |
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SHORT QT SYNDROME 3; SQT3 |
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SHORT RIB-POLYDACTYLY SYNDROME, VERMA-NAUMOFF TYPE |
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SHORT STATURE AND ADVANCED BONE AGE, WITH OR WITHOUT EARLY-ONSET OSTEOARTHRITIS AND/OR OSTEOCHONDRITIS DISSECANS; SSOAOD |
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SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES |
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SHORT STATURE, IDIOPATHIC, X-LINKED; ISS |
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SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED |
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SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS; SOFT |
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