ADENOCARCINOMA OF LUNG, RESPONSE TO TYROS
|
ADENOCARCINOMA OF LUNG, SOMATIC
|
AMYOTROPHIC LATERAL SCLEROSIS 19
|
AORTIC ANEURYSM, FAMILIAL THORACIC 7
|
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4
|
BLADDER CANCER, SOMATIC, INCLUDED
|
BRACHYDACTYLY, TYPE A2
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CAMPTODACTYLY, TALL STATURE, AND HEARING LOSS SYNDROME
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CARDIOFACIOCUTANEOUS SYNDROME 1
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CARDIOFACIOCUTANEOUS SYNDROME 3
|
CARDIOFACIOCUTANEOUS SYNDROME 4
|
CATARACT 6, AGE-RELATED CORTICAL
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CEREBRAL INFARCTION, SUSCEPTIBILITY TO
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CHRONIC MYELOID LEUKEMIA, RESISTANT TO IMATINIB
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COFFIN-LOWRY SYNDROME
|
COFFIN-LOWRY SYNDROME, MILD
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COLON CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6, SOMATIC, INCLUDED
|
COLON CANCER, SOMATIC
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COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6
|
COLORECTAL CANCER, SOMATIC
|
COLORECTAL CANCER, SOMATIC, INCLUDED;;
|
CROUZON SYNDROME
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DEFICIENCY
|
DIABETES MELLITUS, INSULIN-RESISTANT, WITH ACANTHOSIS NIGRICANS
|
DIABETES MELLITUS, NONINSULIN-DEPENDENT
|
DIABETES MELLITUS, TYPE II
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
ESOPHAGEAL CANCER, SOMATIC
|
FG SYNDROME 4
|
FIBRODYSPLASIA OSSIFICANS PROGRESSIVA
|
GASTRIC CANCER, SOMATIC
|
GASTROINTESTINAL STROMAL TUMOR, FAMILIAL
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GASTROINTESTINAL STROMAL TUMOR, SOMATIC
|
GERM CELL TUMOR, SOMATIC
|
GLIOBLASTOMA, SOMATIC
|
GLYCOGEN STORAGE DISEASE IXC
|
HARTSFIELD SYNDROME
|
HEMANGIOMA, CAPILLARY INFANTILE, SOMATIC
|
HEPATOCELLULAR CARCINOMA, CHILDHOOD TYPE, SOMATIC
|
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1
|
HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC, RESISTANT TO IMATINIB
|
HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 5
|
HYPOCHONDROPLASIA
|
HYPOGONADOTROPIC HYPOGONADISM 2 WITH ANOSMIA
|
HYPOGONADOTROPIC HYPOGONADISM 2 WITH ANOSMIA, SUSCEPTIBILITY TO
|
HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA, SUSCEPTIBILITY
|
HYPOGONADOTROPIC HYPOGONADISM 2 WITHOUT ANOSMIA
|
HYPOGONADOTROPIC HYPOGONADISM 2 WITHOUT ANOSMIA, SUSCEPTIBILITY TO
|
IN
|
INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS
|
INSULIN RESISTANCE
|
INSULIN RESISTANCE, INCLUDED
|
IRAK4 DEFICIENCY
|
JUVENILE POLYPOSIS SYNDROME
|
LADD SYNDROME
|
LEUKEMIA, ACUTE LYMPHOBLASTIC, SOMATIC, INCLUDED
|
LEUKEMIA, ACUTE MYELOID
|
LEUKEMIA, ACUTE MYELOID, SOMATIC
|
LEUKEMIA, PHILADELPHIA CHROMOSOME-POSITIVE, RESISTANT TO IMATINIB
|
LOEYS-DIETZ SYNDROME, TYPE 1A
|
LOEYS-DIETZ SYNDROME, TYPE 1B
|
LOEYS-DIETZ SYNDROME, TYPE 1B, INCLUDED
|
LOEYS-DIETZ SYNDROME, TYPE 2A
|
LOEYS-DIETZ SYNDROME, TYPE 2A, INCLUDED
|
LOEYS-DIETZ SYNDROME, TYPE 2B
|
LYMPHEDEMA, HEREDITARY, I
|
LYMPHEDEMA, HEREDITARY, IA
|
LYMPHOMA, NON-HODGKIN, SOMATIC
|
LYMPHOPROLIFERATIVE SYNDROME 1
|
MALFORMATIONS
|
MAST CELL DISEASE, SYSTEMIC
|
MAST CELL LEUKEMIA
|
MASTOCYTOSIS WITH ASSOCIATED HEMATOLOGIC DISORDER, INCLUDED;;
|
MASTOCYTOSIS, ADULT SPORADIC, INCLUDE
|
MASTOCYTOSIS, SPORADIC, CHILDHOOD-ONSET
|
MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME
|
MELANOMA, MALIGNANT, SOMATIC
|
MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA
|
MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA (MICPCH)
|
MENTAL RETARDATION, X-LINKED 19
|
MENTAL RETARDATION, X-LINKED 30
|
MENTAL RETARDATION, X-LINKED, WITH NYSTAGMUS
|
MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA
|
MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB
|
MULTIPLE MYELOMA, SOMATIC, INCLUDED;;
|
MULTIPLE SELF-HEALING SQUAMOUS EPITHELIOMA, SUSCEPTIBILITY TO
|
MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR
|
MYOFIBROMATOSIS, INFANTILE, 1
|
NEPHRONOPHTHISIS 9 (NPHP9)
|
NEUROBLASTOMA, SUSCEPTIBILITY TO, 3
|
NEUROPATHY, HEREDITARY SENSORY, TYPE II
|
NONSMALL CELL LUNG CANCER, RESISTANCE TO TYROSINE KINASE INHIBITOR
|
NONSMALL CELL LUNG CANCER, RESPONSE TO TYROSINE KINASE INHIBITOR IN,
|
NOONAN SYNDROME 7
|
OBESITY, HYPERPHAGIA, AND DEVELOPMENTAL DELAY
|
OGUCHI DISEASE 2
|
OVARIAN CANCER, SOMATIC
|
PARKINSON DISEASE 8, AUTOSOMAL DOMINANT
|
PEUTZ-JEGHERS SYNDROME
|
PFEIFFER SYNDROME
|
PHEOCHROMOCYTOMA, INCLUDED
|
PHEOCHROMOCYTOMA, SOMATIC, IN
|
PIEBALDISM
|
PIEBALDISM WITH SENSORINEURAL DEAFNESS
|
PIEBALDISM, PROGRESSIVE
|
PROSTATE CANCER, PROGRESSION AND METASTASIS OF
|
PULMONARY HYPERTENSION, PRIMARY, 1
|
PULMONARY HYPERTENSION, PRIMARY, 1, WITH HEREDITARY HEMORRHAGIC TELANGIECTASIA
|
PULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED, INCLUDED
|
PULMONARY VENOOCCLUSIVE DISEASE
|
RENAL AGENESIS
|
RENAL CELL CARCINOMA, PAPILLARY, 1
|
RENAL CELL CARCINOMA, PAPILLARY, 1, SOMATIC
|
RETINITIS PIGMENTOSA 38
|
RETINITIS PIGMENTOSA 62
|
RETINITIS PIGMENTOSA 62 (RP62)
|
SADDAN DYSPLASIA
|
SCAPHOCEPHALY, MAXILLARY RETRUSION, AND MENTAL RETARDATION, INCLUDED
|
SELECTIVE T-CELL DEFECT
|
SHORT RIB-POLYDACTYLY SYNDROME 2A (SRPS2A)
|
SHORT RIB-POLYDACTYLY SYNDROME, TYPE IIA
|
SOMATIC
|
SPERMATOCYTIC SEMINOMA, SOMATIC, INCLUDED
|
SPERMATOGENIC FAILURE 5
|
SPINOCEREBELLAR ATAXIA 14
|
SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE
|
T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AUTOIMMUNITY, AND CARDIAC
|
TESTICULAR TUMOR, SOMATIC
|
THANATOPHORIC DYSPLASIA, TYPE I
|
THANATOPHORIC DYSPLASIA, TYPE I, INCLUDED
|
THANATOPHORIC DYSPLASIA, TYPE II
|
THROMBOCYTOPENIA 2
|
THYROID CARCINOMA, FAMILIAL MEDULLARY
|
THYROID CARCINOMA, FAMILIAL MEDULLARY, INCLUDED
|
THYROID CARCINOMA, FOLLICULAR, SOMATIC, INCLUDED
|
THYROID CARCINOMA, PAPILLARY, SOMATIC, INCLUDED;;|
|
THYROID CARCINOMA, SPORADIC MEDULLARY, INCLUDED;;
|
TO
|
VARIANT OF UNKNOWN SIGNIFICANCE
|
VENOUS MALFORMATIONS, MULTIPLE CUTANEOUS AND MUCOSAL
|