| C0002170 |
BXGD000105 |
Alopecia |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C0002395 |
BXGD000111 |
Alzheimer's Disease |
Nervous System Diseases; Mental Disorders |
| C0002736 |
BXGD000127 |
Amyotrophic Lateral Sclerosis |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0004114 |
BXGD000255 |
Astrocytoma |
Neoplasms |
| C0004134 |
BXGD000256 |
Ataxia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0004364 |
BXGD000270 |
Autoimmune Diseases |
Immune System Diseases |
| C0006309 |
BXGD000392 |
Brucellosis |
Infections |
| C0006826 |
BXGD000408 |
Malignant Neoplasms |
Neoplasms |
| C0006849 |
BXGD000413 |
Oral candidiasis |
Infections; Stomatognathic Diseases |
| C0007222 |
BXGD000454 |
Cardiovascular Diseases |
Cardiovascular Diseases |
| C0007570 |
BXGD000467 |
Celiac Disease |
Digestive System Diseases; Nutritional and Metabolic Diseases |
| C0007758 |
BXGD000475 |
Cerebellar Ataxia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0009241 |
BXGD000595 |
Cognition Disorders |
Mental Disorders |
| C0010200 |
BXGD000653 |
Coughing |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases |
| C0011168 |
BXGD000700 |
Deglutition Disorders |
Digestive System Diseases; Otorhinolaryngologic Diseases |
| C0011265 |
BXGD000708 |
Presenile dementia |
Nervous System Diseases; Mental Disorders |
| C0011570 |
BXGD000729 |
Mental Depression |
Behavior and Behavior Mechanisms |
| C0011581 |
BXGD000733 |
Depressive disorder |
Mental Disorders |
| C0011847 |
BXGD000749 |
Diabetes |
Endocrine System Diseases |
| C0011849 |
BXGD000751 |
Diabetes Mellitus |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0011860 |
BXGD000755 |
Diabetes Mellitus, Non-Insulin-Dependent |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0013336 |
BXGD000815 |
Dwarfism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases |
| C0014378 |
BXGD000912 |
Enterovirus Infections |
Infections |
| C0014522 |
BXGD000922 |
Epidermodysplasia Verruciformis |
Infections; Skin and Connective Tissue Diseases |
| C0014544 |
BXGD000926 |
Epilepsy |
Nervous System Diseases |
| C0015544 |
BXGD001003 |
Failure to Thrive |
Pathological Conditions, Signs and Symptoms |
| C0015644 |
BXGD001008 |
Muscular fasciculation |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0015967 |
BXGD001030 |
Fever |
Pathological Conditions, Signs and Symptoms |
| C0016053 |
BXGD001041 |
Fibromyalgia |
Musculoskeletal Diseases; Nervous System Diseases |
| C0016667 |
BXGD001072 |
Fragile X Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0017601 |
BXGD001125 |
Glaucoma |
Eye Diseases |
| C0017636 |
BXGD001131 |
Glioblastoma |
Neoplasms |
| C0017921 |
BXGD001152 |
Glycogen storage disease type II |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0018273 |
BXGD001189 |
Growth Disorders |
Pathological Conditions, Signs and Symptoms |
| C0018524 |
BXGD001200 |
Hallucinations |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms |
| C0018609 |
BXGD001208 |
Hartnup Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nervous System Diseases |
| C0018790 |
BXGD001221 |
Cardiac Arrest |
Cardiovascular Diseases |
| C0018995 |
BXGD001265 |
Hemochromatosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0019196 |
BXGD001301 |
Hepatitis C |
Digestive System Diseases; Infections |
| C0020179 |
BXGD001363 |
Huntington Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders |
| C0020459 |
BXGD001394 |
Hyperinsulinism |
Nutritional and Metabolic Diseases |
| C0020473 |
BXGD001396 |
Hyperlipidemia |
Nutritional and Metabolic Diseases |
| C0020538 |
BXGD001422 |
Hypertensive disease |
Cardiovascular Diseases |
| C0021051 |
BXGD001475 |
Immunologic Deficiency Syndromes |
Immune System Diseases |
| C0021364 |
BXGD001500 |
Male infertility |
Male Urogenital Diseases |
| C0021655 |
BXGD001508 |
Insulin Resistance |
Nutritional and Metabolic Diseases |
| C0022595 |
BXGD001562 |
Keratosis Follicularis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases |
| C0023015 |
BXGD001601 |
Language Disorders |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0023893 |
BXGD001716 |
Liver Cirrhosis, Experimental |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0024141 |
BXGD001740 |
Lupus Erythematosus, Systemic |
Skin and Connective Tissue Diseases; Immune System Diseases |
| C0024408 |
BXGD001768 |
Machado-Joseph Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0025958 |
BXGD001882 |
Microcephaly |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases |
| C0025990 |
BXGD001884 |
Micrognathism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases |
| C0026650 |
BXGD001913 |
Movement Disorders |
Nervous System Diseases |
| C0026769 |
BXGD001930 |
Multiple Sclerosis |
Immune System Diseases; Nervous System Diseases |
| C0026838 |
BXGD001938 |
Muscle Spasticity |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases |
| C0026847 |
BXGD001940 |
Spinal Muscular Atrophy |
Nervous System Diseases |
| C0026848 |
BXGD001941 |
Myopathy |
Musculoskeletal Diseases; Nervous System Diseases |
| C0027121 |
BXGD001973 |
Myositis |
Musculoskeletal Diseases; Nervous System Diseases |
| C0027765 |
BXGD002033 |
nervous system disorder |
Nervous System Diseases |
| C0027868 |
BXGD002053 |
Neuromuscular Diseases |
Nervous System Diseases |
| C0028754 |
BXGD002082 |
Obesity |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C0029401 |
BXGD002135 |
Osteitis Deformans |
Musculoskeletal Diseases |
| C0029453 |
BXGD002154 |
Osteopenia |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0030193 |
BXGD002191 |
Pain |
Pathological Conditions, Signs and Symptoms |
| C0030360 |
BXGD002215 |
Papillon-Lefevre Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases |
| C0030442 |
BXGD002223 |
Progressive bulbar palsy |
Nervous System Diseases |
| C0030552 |
BXGD002238 |
Paresis |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0030567 |
BXGD002240 |
Parkinson Disease |
Nervous System Diseases |
| C0031117 |
BXGD002285 |
Peripheral Neuropathy |
Nervous System Diseases |
| C0032586 |
BXGD002364 |
Polyradiculopathy |
Nervous System Diseases |
| C0033975 |
BXGD002447 |
Psychotic Disorders |
Mental Disorders |
| C0034012 |
BXGD002449 |
Delayed Puberty |
Endocrine System Diseases |
| C0034013 |
BXGD002450 |
Precocious Puberty |
Endocrine System Diseases |
| C0034152 |
BXGD002467 |
Henoch-Schoenlein Purpura |
Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases |
| C0034372 |
BXGD002480 |
Quadriplegia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0035235 |
BXGD002519 |
Respiratory Syncytial Virus Infections |
Infections |
| C0035243 |
BXGD002522 |
Respiratory Tract Infections |
Infections; Respiratory Tract Diseases |
| C0035934 |
BXGD002572 |
Rubinstein-Taybi Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases |
| C0036341 |
BXGD002600 |
Schizophrenia |
Mental Disorders |
| C0036572 |
BXGD002625 |
Seizures |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0038454 |
BXGD002760 |
Cerebrovascular accident |
Nervous System Diseases; Cardiovascular Diseases |
| C0038868 |
BXGD002781 |
Progressive supranuclear palsy |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0039373 |
BXGD002809 |
Tay-Sachs Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0040822 |
BXGD002885 |
Tremor |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0041408 |
BXGD002923 |
Turner Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases; Cardiovascular Diseases |
| C0042267 |
BXGD002974 |
Vaginitis |
Female Urogenital Diseases and Pregnancy Complications |
| C0042928 |
BXGD003014 |
Vocal Cord Paralysis |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C0043116 |
BXGD003028 |
HMN (Hereditary Motor Neuropathy) Proximal Type I |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0085084 |
BXGD003121 |
Motor Neuron Disease |
Nervous System Diseases |
| C0085632 |
BXGD003215 |
Apathy |
Behavior and Behavior Mechanisms |
| C0085633 |
BXGD003216 |
Mood swings |
Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0087012 |
BXGD003318 |
Ataxia, Spinocerebellar |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0151786 |
BXGD003475 |
Muscle Weakness |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases |
| C0154671 |
BXGD003726 |
Degenerative brain disorder |
Nervous System Diseases |
| C0154682 |
BXGD003731 |
Lateral Sclerosis |
Nervous System Diseases |
| C0162429 |
BXGD003942 |
Malnutrition |
Nutritional and Metabolic Diseases |
| C0162534 |
BXGD003953 |
Prion Diseases |
Infections; Nervous System Diseases |
| C0205710 |
BXGD004112 |
Alpers Syndrome (disorder) |
Immune System Diseases; Nervous System Diseases |
| C0220726 |
BXGD004333 |
Diastrophic dysplasia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases |
| C0232197 |
BXGD004536 |
Fibrillation |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0233401 |
BXGD004575 |
Psychiatric symptom |
|
| C0233514 |
BXGD004584 |
Abnormal behavior |
Behavior and Behavior Mechanisms |
| C0233794 |
BXGD004618 |
Memory impairment |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms |
| C0234985 |
BXGD004708 |
Mental deterioration |
Mental Disorders |
| C0235025 |
BXGD004713 |
Peripheral motor neuropathy |
Nervous System Diseases |
| C0235031 |
BXGD004714 |
Neurologic Symptoms |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0235950 |
BXGD004790 |
Zinc deficiency |
Nutritional and Metabolic Diseases |
| C0236642 |
BXGD004815 |
Pick Disease of the Brain |
Nervous System Diseases; Mental Disorders |
| C0242339 |
BXGD005150 |
Dyslipidemias |
Nutritional and Metabolic Diseases |
| C0242422 |
BXGD005163 |
Parkinsonian Disorders |
Nervous System Diseases |
| C0265354 |
BXGD005529 |
CHARGE Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C0268274 |
BXGD005877 |
Gangliosidoses, GM2 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0270736 |
BXGD006096 |
Essential Tremor |
Nervous System Diseases |
| C0271650 |
BXGD006227 |
Impaired glucose tolerance |
Nutritional and Metabolic Diseases |
| C0271742 |
BXGD006254 |
Glucocorticoid deficiency with achalasia |
Digestive System Diseases; Endocrine System Diseases |
| C0282513 |
BXGD006808 |
Primary Progressive Aphasia (disorder) |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders |
| C0282550 |
BXGD006815 |
Persian Gulf Syndrome |
Occupational Diseases |
| C0333463 |
BXGD006954 |
Senile Plaques |
Pathological Conditions, Signs and Symptoms |
| C0338451 |
BXGD007176 |
Frontotemporal dementia |
Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders |
| C0338656 |
BXGD007211 |
Impaired cognition |
Mental Disorders |
| C0338908 |
BXGD007218 |
Mixed anxiety and depressive disorder |
Mental Disorders |
| C0339573 |
BXGD007271 |
Glaucoma, Primary Open Angle |
Eye Diseases |
| C0342751 |
BXGD007542 |
Generalized glycogen storage disease of infants |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0344315 |
BXGD007666 |
Depressed mood |
Behavior and Behavior Mechanisms |
| C0349204 |
BXGD007892 |
Nonorganic psychosis |
Mental Disorders |
| C0349390 |
BXGD007899 |
Non-fluent aphasia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0349588 |
BXGD007933 |
Short stature |
|
| C0375023 |
BXGD007970 |
Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site |
|
| C0376358 |
BXGD007992 |
Malignant neoplasm of prostate |
Neoplasms; Male Urogenital Diseases |
| C0376618 |
BXGD008003 |
Endotoxemia |
Pathological Conditions, Signs and Symptoms; Infections |
| C0391976 |
BXGD008022 |
Pain Disorder |
Mental Disorders |
| C0392678 |
BXGD008063 |
Swallowing problem |
Digestive System Diseases |
| C0393547 |
BXGD008086 |
Bulbospinal Neuronopathy |
Nervous System Diseases |
| C0393911 |
BXGD008155 |
Pure Autonomic Failure |
Nervous System Diseases |
| C0400966 |
BXGD008266 |
Non-alcoholic Fatty Liver Disease |
Digestive System Diseases |
| C0426980 |
BXGD008599 |
Motor symptoms |
|
| C0442874 |
BXGD008814 |
Neuropathy |
Nervous System Diseases |
| C0497327 |
BXGD009061 |
Dementia |
Nervous System Diseases; Mental Disorders |
| C0520679 |
BXGD009101 |
Sleep Apnea, Obstructive |
Respiratory Tract Diseases; Nervous System Diseases |
| C0521170 |
BXGD009131 |
Osteoporotic Fractures |
Wounds and Injuries |
| C0524851 |
BXGD009246 |
Neurodegenerative Disorders |
Nervous System Diseases |
| C0541764 |
BXGD009259 |
Delayed bone age |
|
| C0543859 |
BXGD009298 |
Amyotrophic Lateral Sclerosis, Guam Form |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0553694 |
BXGD009409 |
Oropharyngeal disorders |
Digestive System Diseases; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases |
| C0598589 |
BXGD009667 |
Inherited neuropathies |
Nervous System Diseases |
| C0686377 |
BXGD009834 |
CNS metastases |
Neoplasms; Nervous System Diseases |
| C0751072 |
BXGD010312 |
Frontotemporal Lobar Degeneration |
Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders |
| C0751706 |
BXGD010559 |
Primary Progressive Nonfluent Aphasia |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders |
| C0752121 |
BXGD010669 |
Spinocerebellar Ataxia Type 2 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0752347 |
BXGD010721 |
Lewy Body Disease |
Nervous System Diseases; Mental Disorders |
| C0850024 |
BXGD010896 |
Gluten sensitivity |
Digestive System Diseases; Nutritional and Metabolic Diseases |
| C0878787 |
BXGD011392 |
Growth failure |
|
| C0917814 |
BXGD011418 |
Aphasia, Expressive |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0917981 |
BXGD011423 |
Progressive Muscular Atrophy |
Nervous System Diseases |
| C0920563 |
BXGD011469 |
Insulin Sensitivity |
Nutritional and Metabolic Diseases |
| C0949664 |
BXGD011583 |
Tauopathies |
Nervous System Diseases |
| C1112256 |
BXGD011655 |
Sensorimotor neuropathy |
|
| C1145670 |
BXGD011764 |
Respiratory Failure |
Respiratory Tract Diseases |
| C1261473 |
BXGD011855 |
Sarcoma |
Neoplasms |
| C1263846 |
BXGD011897 |
Attention deficit hyperactivity disorder |
Mental Disorders |
| C1270972 |
BXGD012006 |
Mild cognitive disorder |
Mental Disorders |
| C1306459 |
BXGD012361 |
Primary malignant neoplasm |
Neoplasms |
| C1392786 |
BXGD012978 |
Cognitive changes |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C1458155 |
BXGD013136 |
Mammary Neoplasms |
Neoplasms; Skin and Connective Tissue Diseases |
| C1504404 |
BXGD013141 |
Hippocampal sclerosis |
|
| C1611743 |
BXGD013456 |
Familial (FPAH) |
|
| C1833662 |
BXGD013936 |
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders |
| C1835580 |
BXGD014037 |
Mild postnatal growth retardation |
|
| C1837475 |
BXGD014236 |
Insulin-Like Growth Factor I Deficiency |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C1837728 |
BXGD014259 |
AMYOTROPHIC LATERAL SCLEROSIS 8 (disorder) |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C1839259 |
BXGD014363 |
Bulbo-Spinal Atrophy, X-Linked |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C1839780 |
BXGD014405 |
FRAGILE X TREMOR/ATAXIA SYNDROME |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C1848922 |
BXGD014987 |
Hexosaminidase alpha-Subunit Deficiency (Variant B) |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C1850406 |
BXGD015140 |
NAVAJO NEUROHEPATOPATHY |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C1862939 |
BXGD016144 |
AMYOTROPHIC LATERAL SCLEROSIS 1 |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C1862941 |
BXGD016145 |
Amyotrophic Lateral Sclerosis, Sporadic |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C1864570 |
BXGD016234 |
Insulin insensitivity |
|
| C2146481 |
BXGD016932 |
Bilateral vocal cord paralysis |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C2239176 |
BXGD016965 |
Liver carcinoma |
Digestive System Diseases; Neoplasms |
| C2315100 |
BXGD017021 |
Pediatric failure to thrive |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Mental Disorders |
| C2718017 |
BXGD017522 |
TDP-43 Proteinopathies |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C2919142 |
BXGD017867 |
Short Stature, CTCAE |
|
| C2931845 |
BXGD018076 |
Neurodegeneration with brain iron accumulation (NBIA) |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C3151343 |
BXGD018417 |
SPINOCEREBELLAR ATAXIA 32 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C3469186 |
BXGD018909 |
HEMOCHROMATOSIS, TYPE 1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C3489791 |
BXGD018949 |
Parkinson Disease, Familial, Type 1 |
Nervous System Diseases |
| C3714796 |
BXGD019434 |
Isolated somatotropin deficiency |
|
| C3811918 |
BXGD019664 |
GRN-related frontotemporal dementia |
Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders |
| C3825276 |
BXGD019688 |
Stereotyped behavior (Psychiatry) |
|
| C3887638 |
BXGD019906 |
Failure to thrive in infant |
Pathological Conditions, Signs and Symptoms |
| C3888102 |
BXGD019952 |
Frontotemporal Dementia With Motor Neuron Disease |
Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders |
| C3900122 |
BXGD020112 |
Acid-Labile Subunit Deficiency |
|
| C4011788 |
BXGD020116 |
Behavioral variant of frontotemporal dementia |
Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders |
| C4024896 |
BXGD021461 |
Motor neuron atrophy |
|
| C4072897 |
BXGD022016 |
Decreased serum insulin-like growth factor 1 |
|
| C4082299 |
BXGD022088 |
Bulbar palsy |
Nervous System Diseases |
| C4317045 |
BXGD022719 |
Gluten intolerance |
|
| C4321359 |
BXGD022750 |
Reduced insulin like growth factor binding protein acid labile subunit level |
|
| C4551560 |
BXGD023349 |
Truncal obesity |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C4551686 |
BXGD023391 |
Malignant neoplasm of soft tissue |
Neoplasms |
| C4551993 |
BXGD023469 |
Amyotrophic Lateral Sclerosis, Familial |
Nutritional and Metabolic Diseases; Nervous System Diseases |
| C4721453 |
BXGD023744 |
Peripheral Nervous System Diseases |
Nervous System Diseases |
