ADENOCARCINOMA OF LUNG, SOMATIC
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AORTIC ANEURYSM, FAMILIAL THORACIC 7
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BREAST CANCER, SUSCEPTIBILITY TO
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CARDIOFACIOCUTANEOUS SYNDROME 1
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CARDIOFACIOCUTANEOUS SYNDROME 3
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CARDIOFACIOCUTANEOUS SYNDROME 4
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CHRONIC MYELOID LEUKEMIA, RESISTANT TO IMATINIB
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COFFIN-LOWRY SYNDROME
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COFFIN-LOWRY SYNDROME, MILD
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COLON CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6, SOMATIC, INCLUDED
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COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6
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COLORECTAL CANCER, SOMATIC
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COLORECTAL CANCER, SOMATIC, INCLUDED;;
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CROUZON SYNDROME
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DIABETES MELLITUS, INSULIN-RESISTANT, WITH ACANTHOSIS NIGRICANS
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DIABETES MELLITUS, NONINSULIN-DEPENDENT
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DIABETES MELLITUS, TYPE II
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EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
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ESOPHAGEAL CANCER, SOMATIC
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FG SYNDROME 4
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FIBRODYSPLASIA OSSIFICANS PROGRESSIVA
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GLYCOGEN STORAGE DISEASE IXC
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HEPATOCELLULAR CARCINOMA, CHILDHOOD TYPE, SOMATIC
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HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1
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HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 5
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INSULIN RESISTANCE
|
INSULIN RESISTANCE, INCLUDED
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IRAK4 DEFICIENCY
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LADD SYNDROME
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LEUKEMIA, PHILADELPHIA CHROMOSOME-POSITIVE, RESISTANT TO IMATINIB
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LOEYS-DIETZ SYNDROME, TYPE 1A
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LOEYS-DIETZ SYNDROME, TYPE 1B
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LOEYS-DIETZ SYNDROME, TYPE 1B, INCLUDED
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LOEYS-DIETZ SYNDROME, TYPE 2B
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LYMPHOMA, NON-HODGKIN, SOMATIC
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MALFORMATIONS
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MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME
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MELANOMA, MALIGNANT, SOMATIC
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MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA
|
MENTAL RETARDATION, X-LINKED 19
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MENTAL RETARDATION, X-LINKED 30
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MENTAL RETARDATION, X-LINKED, WITH NYSTAGMUS
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MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA
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MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB
|
MULTIPLE SELF-HEALING SQUAMOUS EPITHELIOMA, SUSCEPTIBILITY TO
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NEUROBLASTOMA, SUSCEPTIBILITY TO, 3
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NEUROPATHY, HEREDITARY SENSORY, TYPE II
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NOONAN SYNDROME 7
|
OGUCHI DISEASE 2
|
PARKINSON DISEASE 8, AUTOSOMAL DOMINANT
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PEUTZ-JEGHERS SYNDROME
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PFEIFFER SYNDROME
|
PHEOCHROMOCYTOMA, INCLUDED
|
PHEOCHROMOCYTOMA, SOMATIC, IN
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PROSTATE CANCER, PROGRESSION AND METASTASIS OF
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RENAL AGENESIS
|
RENAL CELL CARCINOMA, PAPILLARY, 1
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RENAL CELL CARCINOMA, PAPILLARY, 1, SOMATIC
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RETINITIS PIGMENTOSA 62
|
SCAPHOCEPHALY, MAXILLARY RETRUSION, AND MENTAL RETARDATION, INCLUDED
|
SELECTIVE T-CELL DEFECT
|
SHORT RIB-POLYDACTYLY SYNDROME, TYPE IIA
|
SPERMATOGENIC FAILURE 5
|
SPINOCEREBELLAR ATAXIA 14
|
T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AUTOIMMUNITY, AND CARDIAC
|
TESTICULAR TUMOR, SOMATIC
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THROMBOCYTOPENIA 2
|
THYROID CARCINOMA, FAMILIAL MEDULLARY
|
THYROID CARCINOMA, FAMILIAL MEDULLARY, INCLUDED
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THYROID CARCINOMA, FOLLICULAR, SOMATIC, INCLUDED
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THYROID CARCINOMA, PAPILLARY, SOMATIC, INCLUDED;;|
|
THYROID CARCINOMA, SPORADIC MEDULLARY, INCLUDED;;
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VARIANT OF UNKNOWN SIGNIFICANCE
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VENOUS MALFORMATIONS, MULTIPLE CUTANEOUS AND MUCOSAL
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