H2AC18 - H2A clustered histone 18 Gene
Also Known as H2A; H2A.2; H2A/O; H2A/q; H2AFO; H2AC19; H2a-615; HIST2H2AA; HIST2H2AA3
Species: Homo sapiens
About H2AC18
This gene has 1 transcript (splice variant), 91 orthologues and 27 paralogues.
Summary
Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2A family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in a histone cluster on chromosome 1. This gene is one of four histone genes in the cluster that are duplicated; this record represents the centromeric copy. [provided by RefSeq, Aug 2015]
H2AC18 Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_003516.3 | NP_003507.1 | histone H2A type 2-A |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
31759698 | GOA |
| Cellular Component GO Annotation | Evidence | References | Source |
|---|---|---|---|
| located in nucleus |
IDA
IDA: Inferred from direct assay
|
16319397 | GOA |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
histone H2A type 2-A |
|
H2AC18 Antibodies
| Cat. No. | Product Name | Application | Reactivity |
|---|---|---|---|
| HY-P86519 | Histone H2A Antibody (YA6211) | WB, IHC-P, ICC/IF, IP, ELISA | Human, Mouse, Rat |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Riddle Syndrome |
|
|
| Lymph Node Carcinoma |
|
|
| Parasitic Protozoa Infectious Disease |
|
|
| Retinal Cancer |
|
|
| Mature T-Cell And Nk-Cell Lymphoma |
|
|
| Hyperoxaluria, Primary, Type I |
|
|
| Peripheral Nervous System Neoplasm |
|
|
| Autonomic Nervous System Neoplasm |
|
|
| Histone Mutated Tumor |
|
|
| Toxic Encephalopathy |
|
|
| Lymphatic System Disease |
|
|
| Splenic Disease |
|
|
| Male Reproductive System Disease |
|
|
| Primary Hyperoxaluria |
|
|
| Acute Erythroid Leukemia |
|
|
| Ovarian Carcinosarcoma |
|
|
| Sensory System Disease |
|
|
| Physical Disorder |
|
|
| Bone Marrow Cancer |
|
|
| Autoimmune Myocarditis |
|
|
| Specific Developmental Disorder |
|
|
| Paraphilia Disorder |
|
|
| Carbohydrate Metabolic Disorder |
|
|
| Thoracic Cancer |
|
|
| Drug-Induced Lupus Erythematosus |
|
|
| Lymphatic System Cancer |
|
|
| Exhibitionism |
|
|
| Uterine Corpus Cancer |
|
|
| Autoimmune Disease Of Musculoskeletal System |
|
|
| Systemic Scleroderma |
|
|
| Endocrine System Disease |
|
|
| Fetishism |
|
|
| Connective Tissue Cancer |
|
|
| Childhood Brain Stem Glioma |
|
|
| Alpha Thalassemia-X-Linked Intellectual Disability Syndrome |
|
|
| Infratentorial Cancer |
|
|
| Uterine Body Mixed Cancer |
|
|
| Malignant Ovarian Surface Epithelial-Stromal Neoplasm |
|
|
| Biotin Deficiency |
|
|
| Integumentary System Disease |
|
|
| Inherited Metabolic Disorder |
|
|
| Reproductive System Disease |
|
|
| Rumination Disorder |
|
|
| Germ Cell And Embryonal Cancer |
|
|
| Xeroderma Pigmentosum, Complementation Group C |
|
|
| Acquired Metabolic Disease |
|
|
| Central Nervous System Cancer |
|
|
| Chromosomal Deletion Syndrome |
|
|
| Muscular Disease |
|
|
| Ocular Cancer |
|
|
| Mixed Cell Type Cancer |
|
|
| Bone Inflammation Disease |
|
|
| Cogan-Reese Syndrome |
|
|
| Disease Of Mental Health |
|
|
| Immune System Disease |
|
|
| Fetal Alcohol Spectrum Disorder |
|
|
| Ovary Epithelial Cancer |
|
|
| Primary Bacterial Infectious Disease |
|
|
| Ruijs-Aalfs Syndrome |
|
|
| Chromosome 16p13.3 Deletion Syndrome, Proximal |
|
|
| Chromosomal Disease |
|
|
| Leukocyte Disease |
|
|
| Coccidiosis |
|
|
| Chromosomal Duplication Syndrome |
|
|
| Seckel Syndrome 2 |
|
|
| Female Reproductive System Disease |
|
|
| Male Reproductive Organ Cancer |
|
|
| Xeroderma Pigmentosum, Complementation Group G |
|
|
| Adult Syndrome |
|
|
| Cartilage-Hair Hypoplasia |
|
|
| Retinitis Pigmentosa 20 |
|
|
| Skin Carcinoma |
|
|
| Connective Tissue Benign Neoplasm |
|
|
| Rapp-Hodgkin Syndrome |
|
|
| Glucose Metabolism Disease |
|
|
| Cell Type Benign Neoplasm |
|
|
| Nut Midline Carcinoma |
|
|
| Microphthalmia, Syndromic 2 |
|
|
| Diffuse Midline Glioma, H3 K27m-Mutant |
|
|
| Otopalatodigital Syndrome, Type I |
|
|
| Retinitis Pigmentosa 18 |
|
|
| Xeroderma Pigmentosum Group E |
|
|
| Autosomal Recessive Cerebellar Ataxia |
|
|
| Floating-Harbor Syndrome |
|
|
| Muscle Tissue Disease |
|
|
| Central Nervous System Benign Neoplasm |
|
|
| Epilepsy, Idiopathic Generalized 2 |
|
|
| Mucocutaneous Leishmaniasis |
|
|
| Spinal Disease |
|
|
| Miliaria |
|
|
| Gastrointestinal System Disease |
|
|
| Urinary System Disease |
|
|
| Disease By Infectious Agent |
|
|
| Large Intestine Cancer |
|
|
| Alexithymia |
|
|
| Respiratory System Disease |
|
|
| Xeroderma Pigmentosum, Variant Type |
|
|
| Anus Benign Neoplasm |
|
|
| Bone Sarcoma |
|
|
| Amyotrophic Lateral Sclerosis 4, Juvenile |
|
|
| Amino Acid Metabolic Disorder |
|
|
| Malignant Exocrine Pancreas Neoplasm |
|
|
| Colonic Disease |
|
|
| Microcephaly 11, Primary, Autosomal Recessive |
|
|
| Ovarian Clear Cell Adenocarcinoma |
|
|
| Syndromic Microphthalmia |
|
|
| Kleefstra Syndrome |
|
|
| 46,Xy Sex Reversal 6 |
|
|
| Schizophrenia 7 |
|
|
| Ovarian Small Cell Carcinoma |
|
|
| Low Grade Glioma |
|
|
| Immunodeficiency 15a |
|
|
| Bjornstad Syndrome |
|
|
| Epithelial-Stromal Tgfbi Dystrophy |
|
|
| Uveal Disease |
|
|
| Respiratory System Cancer |
|
|
| Cerebellar Disease |
|
|
| Mature B-Cell Neoplasm |
|
|
| Autoimmune Disease Of Endocrine System |
|
|
| Autosomal Dominant Intellectual Developmental Disorder |
|
|
| Sleeping Sickness |
|
|
| Autoimmune Disease Of Central Nervous System |
|
|
| Xeroderma Pigmentosum, Complementation Group A |
|
|
| Intestinal Disease |
|
|
| Autoimmune Disease Of Cardiovascular System |
|
|
| Cowden Syndrome 5 |
|
|
| Spinal Cord Disease |
|
|
| Immune-Complex Glomerulonephritis |
|
|
| Felty Syndrome |
|
|
| Spinocerebellar Ataxia Type 1 With Axonal Neuropathy |
|
|
| Extrinsic Cardiomyopathy |
|
|
| Necrotizing Fasciitis |
|
|
| Arteries, Anomalies Of |
|
|
| Cockayne Syndrome B |
|
|
| Ovarian Disease |
|
|
| Chondroblastoma |
|
|
| Autoimmune Disease Of Gastrointestinal Tract |
|
|
| Crest Syndrome |
|
|
| Chromosome 2q37 Deletion Syndrome |
|
|
| Uterine Anomalies |
|
|
| Anus Cancer |
|
|
| Microphthalmia, Syndromic 1 |
|
|
| Testicular Disease |
|
|
| Weaver Syndrome |
|
|
| Blood Coagulation Disease |
|
|
| Gastrointestinal System Cancer |
|
|
| Acute Myocarditis |
|
|
| Ovary Adenocarcinoma |
|
|
| Central Nervous System Disease |
|
|
| Retinal Disease |
|
|
| Endometrioid Ovary Carcinoma |
|
|
| Coronavirus Infectious Disease |
|
|
| Narcissistic Personality Disorder |
|
|
| Mature Teratoma |
|
|
| Uv-Sensitive Syndrome |
|
|
| Lens Disease |
|
|
| Oropharynx Cancer |
|
|
| Kabuki Syndrome 1 |
|
|
| Thymus Gland Disease |
|
|
| Overnutrition |
|
|
| D-2-Hydroxyglutaric Aciduria 2 |
|
|
| Malignant Astrocytoma |
|
|
| Bladder Disease |
|
|
| Immunodeficiency 15b |
|
|
| Bone Cancer |
|
|
| Sporadic Breast Cancer |
|
|
| Bronchial Disease |
|
|
| Ohdo Syndrome |
|
|
| Anus Disease |
|
|
| Endocrine Gland Cancer |
|
|
| Eye Degenerative Disease |
|
|
| Heart Block, Congenital |
|
|
| Spinocerebellar Ataxia 7 |
|
|
| Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome |
|
|
| Ogden Syndrome |
|
|
| Orchitis |
|
|
| Schopf-Schulz-Passarge Syndrome |
|
|
| Chronic Atrial And Intestinal Dysrhythmia |
|
|
| Clear Cell Chondrosarcoma |
|
|
| Thymus Cancer |
|
|
| Cervix Disease |
|
|
| Autoimmune Disease Of Skin And Connective Tissue |
|
|
| Epiphyseal Dysplasia, Multiple, 2 |
|
|
| Multicentric Castleman Disease |
|
|
| Multiple Epiphyseal Dysplasia Due To Collagen 9 Anomaly |
|
|
| Germ Cell Cancer |
|
|
| Salivary Gland Carcinoma |
|
|
| Bainbridge-Ropers Syndrome |
|
|
| Bone Osteosarcoma |
|
|
| Pancreas Disease |
|
|
| Colorectal Adenocarcinoma |
|
|
| Autoimmune Vasculitis |
|
|
| Phobia, Specific |
|
|
| Substance Dependence |
|
|
| Otopalatodigital Syndrome Spectrum Disorder |
|
|
| Mental Depression |
|
|
| Kleefstra Syndrome 1 |
|
|
| Chronic Leukemia |
|
|
| Brain Stem Cancer |
|
|
| Spherocytosis, Type 4 |
|
|
| Bile Duct Cancer |
|
|
| Noonan Syndrome 11 |
|
|
| Cervix Carcinoma |
|
|
| Bile Duct Adenocarcinoma |
|
|
| Primary Cutaneous T-Cell Non-Hodgkin Lymphoma |
|
|
| Brain Glioma |
|
|
| Estrogen-Receptor Negative Breast Cancer |
|
|
| Rhabdoid Cancer |
|
|
| Bone Development Disease |
|
|
| Lattice Corneal Dystrophy |
|
|
| Cleft Palate, Isolated |
|
|
| Cockayne Syndrome A |
|
|
| Hereditary Ataxia |
|
|
| Alcohol Use Disorder |
|
|
| Choline Deficiency Disease |
|
|
| Severe Combined Immunodeficiency With Sensitivity To Ionizing Radiation |
|
|
| Hematologic Cancer |
|
|
| Breast Adenocarcinoma |
|
|
| Substance Abuse |
|
|
| Thyroid Gland Disease |
|
|
| Pleural Cancer |
|
|
| Methemoglobinemia And Ambiguous Genitalia |
|
|
| Ovarian Clear Cell Carcinoma |
|
|
| Aicardi-Goutieres Syndrome |
|
|
| Spinocerebellar Ataxia, Autosomal Recessive, With Axonal Neuropathy 2 |
|
|
| Endometrial Stromal Tumor |
|
|
| Breast Disease |
|
|
| Endemic Typhus |
|
|
| Complement Component 5 Deficiency |
|
|
| Muscle Cancer |
|
|
| Fanconi Anemia, Complementation Group I |
|
|
| Cystic Echinococcosis |
|
|
| Adult T-Cell Leukemia/Lymphoma |
|
|
| Autoimmune Disease Of Exocrine System |
|
|
| Amelogenesis Imperfecta, Type Ig |
|
|
| Prostate Disease |
|
|
| Wolf-Hirschhorn Syndrome |
|
|
| Anal Squamous Cell Carcinoma |
|
|
| Roberts-Sc Phocomelia Syndrome |
|
|
| Skeletal Muscle Cancer |
|
|
| Giardiasis |
|
|
| Goodpasture Syndrome |
|
|
| Teeth Hard Tissue Disease |
|
|
| Somatoform Disorder |
|
|
| Pervasive Developmental Disorder |
|
|
| Salivary Gland Disease |
|
|
| Sting-Associated Vasculopathy With Onset In Infancy |
|
|
| Paranoid Schizophrenia |
|
|
| Parasitic Helminthiasis Infectious Disease |
|
|
| Post-Traumatic Stress Disorder |
|
|
| Gastrointestinal System Benign Neoplasm |
|
|
| Fungal Infectious Disease |
|
|
| Skin Atrophy |
|
|
| Head And Neck Cancer |
|
|
| Castleman Disease |
|
|
| Macular Degeneration, Age-Related, 1 |
|
|
| Atrichia With Papular Lesions |
|
|
| Peripheral T-Cell Lymphoma |
|
|
| Cardiovascular Organ Benign Neoplasm |
|
|
| Respiratory System Benign Neoplasm |
|
|
| Autoimmune Disease Of Urogenital Tract |
|
|
| Localized Scleroderma |
|
|
| Plague |
|
|
| Orofacial Cleft |
|
|
| Hair Disease |
|
|
| Ebola Hemorrhagic Fever |
|
|
| Charge Syndrome |
|
|
| Cutaneous Leishmaniasis |
|
|
| Colorectal Cancer |
|
|
| Telangiectasis |
|
|
| Listeriosis |
|
|
| Mast Cell Neoplasm |
|
|
| Fetal Alcohol Syndrome |
|
|
| Intestinal Benign Neoplasm |
|
|
| West Nile Encephalitis |
|
|
| Peripheral Nervous System Disease |
|
|
| Alpha-Thalassemia |
|
|
| Blood Platelet Disease |
|
|
| Synovium Cancer |
|
|
| Lung Adenoma |
|
|
| Mantle Cell Lymphoma |
|
|
| Meier-Gorlin Syndrome 1 |
|
|
| Generalized Anxiety Disorder |
|
|
| Endocervical Carcinoma |
|
|
| Lipid Storage Disease |
|
|
| Commensal Bacterial Infectious Disease |
|
|
| Learning Disability |
|
|
| Diffuse Astrocytoma |
|
|
| Melanoma In Congenital Melanocytic Nevus |
|
|
| Clark-Baraitser Syndrome |
|
|
| Seckel Syndrome |
|
|
| Inflammatory Bowel Disease 1 |
|
|
| Sotos Syndrome |
|
|
| Pleural Disease |
|
|
| Exanthem |
|
|
| Visceral Leishmaniasis |
|
|
| Epithelioid Sarcoma |
|
|
| Renal Cell Carcinoma, Nonpapillary |
|
|
| Anogenital Venereal Wart |
|
|
| Lung Large Cell Carcinoma |
|
|
| Coffin-Lowry Syndrome |
|
|
| Bile Duct Disease |
|
|
| Suppression Of Tumorigenicity 12 |
|
|
| Trypanosomiasis |
|
|
| Xeroderma Pigmentosum, Complementation Group F |
|
|
| Silver-Russell Syndrome 1 |
|
|
| Retinal Vascular Disease |
|
|
| Leukemia, Acute Monocytic |
|
|
| Estrogen-Receptor Positive Breast Cancer |
|
|
| Melanoma, Uveal |
|
|
| Peritoneum Cancer |
|
|
| Opportunistic Mycosis |
|
|
| Proliferative Glomerulonephritis |
|
|
| Nijmegen Breakage Syndrome |
|
|
| Retinitis Pigmentosa 11 |
|
|
| Lymphoma, Non-Hodgkin, Familial |
|
|
| Connective Tissue Disease |
|
|
| Brain Cancer |
|
|
| Biliary Tract Disease |
|
|
| Human Immunodeficiency Virus Infectious Disease |
|
|
| Autosomal Dominant Cerebellar Ataxia |
|
|
| Intrinsic Cardiomyopathy |
|
|
| Eosinophilia-Myalgia Syndrome |
|
|
| Pre-Malignant Neoplasm |
|
|
| Kaposi Sarcoma |
|
|
| Actinic Keratosis |
|
|
| Upper Respiratory Tract Disease |
|
|
| Stomach Disease |
|
|
| Rectal Disease |
|
|
| Lymph Node Disease |
|
|
| Cerebrovascular Disease |
|
|
| Oral Cavity Cancer |
|
|
| Amyotrophic Lateral Sclerosis Type 6 |
|
|
| Endogenous Depression |
|
|
| Dental Pulp Disease |
|
|
| Demyelinating Disease |
|
|
| Mulibrey Nanism |
|
|
| Uterine Carcinosarcoma |
|
|
| Thyroid Gland Cancer |
|
|
| Lung Cancer |
|
|
| Neural Tube Defects |
|
|
| Pfeiffer Syndrome |
|
|
| Peptic Ulcer Disease |
|
|
| Coloboma Of Macula |
|
|
| Mood Disorder |
|
|
| Immunodeficiency With Hyper-Igm, Type 2 |
|
|
| Psychotic Disorder |
|
|
| Heart Septal Defect |
|
|
| Hereditary Sensory Neuropathy |
|
|
| Ovarian Serous Carcinoma |
|
|
| Immune Deficiency Disease |
|
|
| Sexual Health Disorder |
|
|
| Chronic Myelomonocytic Leukemia |
|
|
| Hutchinson-Gilford Progeria Syndrome |
|
|
| Fanconi Anemia, Complementation Group D2 |
|
|
| Acrofacial Dysostosis 1, Nager Type |
|
|
| Combined Immunodeficiency |
|
|
| Peripheral Vascular Disease |
|
|
| Cecal Disease |
|
|
| Dengue Disease |
|
|
| Corneal Disease |
|
|
| Bone Disease |
|
|
| Fanconi Anemia, Complementation Group A |
|
|
| Spermatogenic Failure |
|
|
| Viral Infectious Disease |
|
|
| Endometrial Stromal Sarcoma |
|
|
| Pharynx Cancer |
|
|
| Bone Remodeling Disease |
|
|
| Trichothiodystrophy |
|
|
| Esophageal Disease |
|
|
| Deficiency Anemia |
|
|
| Nutritional Deficiency Disease |
|
|
| Aortic Disease |
|
|
| Hashimoto Thyroiditis |
|
|
| Skin Melanoma |
|
|
| Cryptosporidiosis |
|
|
| Microcephaly 5, Primary, Autosomal Recessive |
|
|
| Ectodermal Dysplasia |
|
|
| Eye Disease |
|
|
| Cocaine Abuse |
|
|
| Collagen Disease |
|
|
| Serous Cystadenocarcinoma |
|
|
| Placenta Disease |
|
|
| Bacterial Infectious Disease |
|
|
| Autoimmune Disease Of Blood |
|
|
| Primary Microcephaly |
|
|
| Nervous System Disease |
|
|
| Aplastic Anemia |
|
|
| Coffin-Siris Syndrome 1 |
|
|
| Heart Disease |
|
|
| Dysentery |
|
|
| Blood Protein Disease |
|
|
| Endocrine Organ Benign Neoplasm |
|
|
| Bone Resorption Disease |
|
|
| Paine Syndrome |
|
|
| Bone Giant Cell Tumor |
|
|
| Childhood Medulloblastoma |
|
|
| Esophageal Cancer |
|
|
| Immunodeficiency With Hyper-Igm, Type 1 |
|
|
| T-Cell Prolymphocytic Leukemia |
|
|
| Cardiovascular System Disease |
|
|
| Biliary Tract Cancer |
|
|
| Atrial Heart Septal Defect |
|
|
| Wilms Tumor 1 |
|
|
| Degeneration Of Macula And Posterior Pole |
|
|
| Mouth Disease |
|
|
| Primary Autosomal Recessive Microcephaly |
|
|
| Cardiomyopathy, Dilated, 1a |
|
|
| Cornelia De Lange Syndrome |
|
|
| Anaplastic Astrocytoma |
|
|
| Testicular Cancer |
|
|
| Eating Disorder |
|
|
| Ocular Melanoma |
|
|
| Kidney Cancer |
|
|
| Emery-Dreifuss Muscular Dystrophy |
|
|
| Rothmund-Thomson Syndrome, Type 2 |
|
|
| Hereditary Breast Ovarian Cancer Syndrome |
|
|
| Skin Disease |
|
|
| Lynch Syndrome |
|
|
| Colorectal Adenoma |
|
|
| Machado-Joseph Disease |
|
|
| Lung Disease |
|
|
| Intrahepatic Cholangiocarcinoma |
|
|
| Isolated Growth Hormone Deficiency |
|
|
| Isolated Growth Hormone Deficiency, Type Ia |
|
|
| Heart Valve Disease |
|
|
| Adult Respiratory Distress Syndrome |
|
|
| Urinary Tract Infection |
|
|
| Chronic Fatigue Syndrome |
|
|
| Nasopharyngeal Disease |
|
|
| Lysosomal Storage Disease |
|
|
| Shigellosis |
|
|
| Tonsil Cancer |
|
|
| Crohn'S Disease |
|
|
| High Grade Glioma |
|
|
| Sarcoma, Synovial |
|
|
| Fallopian Tube Disease |
|
|
| Leukemia, Acute Myeloid |
|
|
| Diffuse Large B-Cell Lymphoma |
|
|
| Systemic Lupus Erythematosus |
|
|
| Phobic Disorder |
|
|
| Agnosia |
|
|
| Respiratory Failure |
|
|
| Bladder Cancer |
|
|
| Microvascular Complications Of Diabetes 5 |
|
|
| Lymphoma, Hodgkin, Classic |
|
|
| Disorder Of Sexual Development |
|
|
| Ovarian Cystadenocarcinoma |
|
|
| Phenylketonuria |
|
|
| Interstitial Lung Disease |
|
|
| Supratentorial Cancer |
|
|
| Tobacco Addiction |
|
|
| Dysostosis |
|
|
| Transient Neonatal Diabetes Mellitus |
|
|
| Refractive Error |
|
|
| Pulmonary Disease, Chronic Obstructive |
|
|
| Mycobacterium Tuberculosis 1 |
|
|
| Childhood Leukemia |
|
|
| Allergic Disease |
|
|
| Multiple Endocrine Neoplasia, Type I |
|
|
| Myeloproliferative Neoplasm |
|
|
| Hemolytic Anemia |
|
|
| Pancreatic Ductal Adenocarcinoma |
|
|
| Myxofibrosarcoma |
|
|
| Mineral Metabolism Disease |
|
|
| Mesothelioma, Malignant |
|
|
| Reproductive Organ Benign Neoplasm |
|
|
| Beckwith-Wiedemann Syndrome |
|
|
| Dyskeratosis Congenita |
|
|
| Movement Disease |
|
|
| Endometrial Cancer |
|
|
| Sleep Disorder |
|
|
| Male Infertility |
|
|
| Von Hippel-Lindau Syndrome |
|
|
| Ventricular Septal Defect |
|
|
| Colonic Benign Neoplasm |
|
|
| Pancreatic Cancer |
|
|
| Ovarian Serous Cystadenocarcinoma |
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| Leukemia, Acute Lymphoblastic |
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| Amelogenesis Imperfecta |
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| Omenn Syndrome |
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| Choreatic Disease |
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| Pituitary Gland Disease |
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| Celiac Disease 1 |
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| Sphingolipidosis |
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| Vascular Disease |
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| Dementia, Lewy Body |
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| Ovarian Cancer |
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| Amyotrophic Lateral Sclerosis 1 |
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| Myelodysplastic Syndrome |
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| Rectum Cancer |
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| Leukemia, Chronic Myeloid |
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| Motor Neuron Disease |
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| Congenital Nervous System Abnormality |
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| Potocki-Shaffer Syndrome |
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| Hepatocellular Carcinoma |
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| Prostate Cancer |
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| Migraine With Or Without Aura 1 |
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| Alcohol Dependence |
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| Angelman Syndrome |
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| Adrenal Cortex Disease |
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| Atypical Teratoid Rhabdoid Tumor |
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| Body Mass Index Quantitative Trait Locus 11 |
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| Aortic Valve Disease 2 |
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| Metal Metabolism Disorder |
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| Williams-Beuren Syndrome |
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| Huntington Disease |
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| Prader-Willi Syndrome |
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| Heart Conduction Disease |
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| Li-Fraumeni Syndrome |
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| Severe Combined Immunodeficiency |
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| Lymphangioma |
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| Aortic Aneurysm, Familial Abdominal, 1 |
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| Brachydactyly |
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| T-Cell Acute Lymphoblastic Leukemia |
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| Myeloma, Multiple |
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| Gastric Cancer |
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| Sickle Cell Anemia |
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| Leukemia, Chronic Lymphocytic |
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| Primary Biliary Cholangitis |
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| Lung Squamous Cell Carcinoma |
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| Pancytopenia |
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| Oral Squamous Cell Carcinoma |
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| Lipid Metabolism Disorder |
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| Alzheimer Disease, Familial, 1 |
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| Breast Cancer |
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| Cerebral Degeneration |
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| Attention Deficit-Hyperactivity Disorder |
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| Essential Thrombocythemia |
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| Acute Promyelocytic Leukemia |
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| Ewing Sarcoma |
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| Cystic Kidney Disease |
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| Maturity-Onset Diabetes Of The Young |
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| Gastrointestinal Stromal Tumor |
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| Lung Cancer Susceptibility 3 |
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| Parkinson Disease, Late-Onset |
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| Squamous Cell Carcinoma, Head And Neck |
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| Basal Cell Carcinoma |
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| Meningioma, Familial |
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| Lipoprotein Quantitative Trait Locus |
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| Frontotemporal Dementia |
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| Osteochondrodysplasia |
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| Neuromuscular Disease |
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| Microphthalmia |
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| Tetralogy Of Fallot |
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| Dilated Cardiomyopathy |
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| Hypertrophic Cardiomyopathy |
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| Myopathy |
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| Type 2 Diabetes Mellitus |
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| Behcet Syndrome |
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| Polycystic Kidney Disease |
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| Interstitial Lung Disease 2 |
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| Hypertension, Essential |
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| Cerebral Palsy |
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| Retinitis Pigmentosa |
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| Charcot-Marie-Tooth Disease |
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| Microcephaly |
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