Hereditary Lesion

Preferred Label : Hereditary Lesion;

NCIt definition : A pathologic process inherited in a familial pattern.;

Details

Origin ID

C54062;

UMLS CUI

C1708351;

Semantic type(s)
- Finding [UMLS semantic type]
is_finding_of_disease
- Acute Lymphoblastic Leukemia, Susceptibility to, 3 [NCIt concept]
- Acute Myeloid Leukemia with Germline CEBPA Mutation [NCIt concept]
- Aggravated Neurofibromatosis [NCIt concept]
- Ataxia Telangiectasia Syndrome [NCIt concept]
- Attenuated Familial Adenomatous Polyposis [NCIt concept]
- Autosomal Dominant Optic Atrophy [NCIt concept]
- BAP1 Tumor Predisposition Syndrome [NCIt concept]
- BRCA-Associated Breast Carcinoma [NCIt concept]
- BRCA-Associated Malignant Neoplasm [NCIt concept]
- BRCA-Associated Ovarian Carcinoma [NCIt concept]
- BRCA1-Associated Hereditary Breast and Ovarian Cancer Syndrome [NCIt concept]
- BRCA1/2-Associated Hereditary Breast and Ovarian Cancer Syndrome [NCIt concept]
- BRCA2-Associated Hereditary Breast and Ovarian Cancer Syndrome [NCIt concept]
- Bannayan-Riley-Ruvalcaba Syndrome [NCIt concept]
- Beckwith-Wiedemann Syndrome [NCIt concept]
- Bietti Crystalline Corneoretinal Dystrophy [NCIt concept]
- Birt-Hogg-Dube Syndrome [NCIt concept]
- Bloom Syndrome [NCIt concept]
- CDC73-Related Neoplastic Syndrome [NCIt concept]
- CDH1-Associated Breast Carcinoma Syndrome [NCIt concept]
- CHEK2-Associated Li-Fraumeni-Like Syndrome [NCIt concept]
- Carney Complex [NCIt concept]
- Carney-Stratakis Syndrome [NCIt concept]
- Cherubism [NCIt concept]
- Cobb Syndrome [NCIt concept]
- Cone-Rod Dystrophy 2 [NCIt concept]
- Congenital Pure Red Cell Aplasia [NCIt concept]
- Constitutional Mismatch Repair Deficiency Syndrome [NCIt concept]
- Cowden Syndrome [NCIt concept]
- Cutaneous Malignant Melanoma 2 [NCIt concept]
- Diamond-Blackfan Anemia 1 [NCIt concept]
- Diamond-Blackfan Anemia 10 [NCIt concept]
- Diamond-Blackfan Anemia 11 [NCIt concept]
- Diamond-Blackfan Anemia 3 [NCIt concept]
- Diamond-Blackfan Anemia 4 [NCIt concept]
- Diamond-Blackfan Anemia 5 [NCIt concept]
- Diamond-Blackfan Anemia 6 [NCIt concept]
- Diamond-Blackfan Anemia 7 [NCIt concept]
- Diamond-Blackfan Anemia 8 [NCIt concept]
- Diamond-Blackfan Anemia 9 [NCIt concept]
- Dysplastic Nevus Syndrome [NCIt concept]
- ELP1-Medulloblastoma Syndrome [NCIt concept]
- Familial Adenomatous Polyposis [NCIt concept]
- Familial Amyloidosis [NCIt concept]
- Familial Hemophagocytic Lymphohistiocytosis [NCIt concept]
- Familial Hemophagocytic Lymphohistiocytosis Type 2 [NCIt concept]
- Familial Hemophagocytic Lymphohistiocytosis Type 3 [NCIt concept]
- Familial Hemophagocytic Lymphohistiocytosis Type 4 [NCIt concept]
- Familial Hemophagocytic Lymphohistiocytosis Type 5 [NCIt concept]
- Familial Primary Localized Cutaneous Amyloidosis-1 [NCIt concept]
- Familial Testicular Germ Cell Tumor [NCIt concept]
- Familial Waldenstrom Macroglobulinemia [NCIt concept]
- Fanconi Anemia [NCIt concept]
- Fanconi Anemia, Complementation Group A [NCIt concept]
- Fanconi Anemia, Complementation Group B [NCIt concept]
- Fanconi Anemia, Complementation Group C [NCIt concept]
- Fanconi Anemia, Complementation Group D1 [NCIt concept]
- Fanconi Anemia, Complementation Group D2 [NCIt concept]
- Fanconi Anemia, Complementation Group E [NCIt concept]
- Fanconi Anemia, Complementation Group F [NCIt concept]
- Fanconi Anemia, Complementation Group G [NCIt concept]
- Fanconi Anemia, Complementation Group I [NCIt concept]
- Fanconi Anemia, Complementation Group J [NCIt concept]
- Fanconi Anemia, Complementation Group L [NCIt concept]
- Fanconi Anemia, Complementation Group N [NCIt concept]
- Fanconi Anemia, Complementation Group O [NCIt concept]
- Gardner Syndrome [NCIt concept]
- Gastric Adenocarcinoma and Proximal Polyposis of the Stomach [NCIt concept]
- Glucagon Cell Hyperplasia and Neoplasia [NCIt concept]
- Hematologic Neoplasm Associated with Down Syndrome [NCIt concept]
- Hematologic Neoplasm with Germline ANKRD26 Mutation [NCIt concept]
- Hematologic Neoplasm with Germline DDX41 Mutation [NCIt concept]
- Hematologic Neoplasm with Germline ETV6 Mutation [NCIt concept]
- Hematologic Neoplasm with Germline GATA2 Mutation [NCIt concept]
- Hematologic Neoplasm with Germline Predisposition [NCIt concept]
- Hematologic Neoplasm with Germline Predisposition Associated with Inherited Bone Marrow Failure Syndrome [NCIt concept]
- Hematologic Neoplasm with Germline Predisposition Associated with Telomerase Biology Disorder [NCIt concept]
- Hematologic Neoplasm with Germline Predisposition Associated with a Constitutional Disorder Affecting Multiple Organ Systems [NCIt concept]
- Hematologic Neoplasm with Germline Predisposition Associated with a Constitutional Platelet Disorder [NCIt concept]
- Hematologic Neoplasm with Germline Predisposition without a Constitutional Disorder Affecting Multiple Organ Systems [NCIt concept]
- Hematologic Neoplasm with Germline RUNX1 Mutation [NCIt concept]
- Hematologic Neoplasm with Germline SAMD9 Mutation [NCIt concept]
- Hematologic Neoplasm with Germline SAMD9L Mutation [NCIt concept]
- Hemolytic Anemia due to Membrane Defect [NCIt concept]
- Hereditary Adrenal Gland Pheochromocytoma [NCIt concept]
- Hereditary Atypical Mole Melanoma Syndrome [NCIt concept]
- Hereditary Benign Intraepithelial Dyskeratosis [NCIt concept]
- Hereditary Breast Carcinoma [NCIt concept]
- Hereditary Clear Cell Renal Cell Carcinoma [NCIt concept]
- Hereditary Colon Carcinoma [NCIt concept]
- Hereditary Colorectal Cancer Syndrome [NCIt concept]
- Hereditary Colorectal Cancer Type X [NCIt concept]
- Hereditary Corneal Dystrophy [NCIt concept]
- Hereditary Elliptocytosis [NCIt concept]
- Hereditary Fallopian Tube Carcinoma [NCIt concept]
- Hereditary Female Breast Carcinoma [NCIt concept]
- Hereditary Gastric Diffuse Adenocarcinoma [NCIt concept]
- Hereditary Gastrointestinal Stromal Tumor [NCIt concept]
- Hereditary Glomangioma [NCIt concept]
- Hereditary Hemolytic Anemia [NCIt concept]
- Hereditary Hemorrhagic Telangiectasia [NCIt concept]
- Hereditary Isolated Hyperparathyroidism [NCIt concept]
- Hereditary Kidney Oncocytoma [NCIt concept]
- Hereditary Kidney Wilms Tumor [NCIt concept]
- Hereditary Leiomyomatosis and Renal Cell Carcinoma [NCIt concept]
- Hereditary Male Breast Carcinoma [NCIt concept]
- Hereditary Malignant Neoplasm [NCIt concept]
- Hereditary Malignant Urinary System Neoplasm [NCIt concept]
- Hereditary Melanoma [NCIt concept]
- Hereditary Meningioma [NCIt concept]
- Hereditary Multiple Exostoses [NCIt concept]
- Hereditary Myelodysplastic Syndrome [NCIt concept]
- Hereditary Neoplastic Syndrome [NCIt concept]
- Hereditary Neuroblastoma [NCIt concept]
- Hereditary Nonmedullary Thyroid Gland Carcinoma [NCIt concept]
- Hereditary Nonpolyposis Colorectal Cancer Syndrome [NCIt concept]
- Hereditary Optic Atrophy [NCIt concept]
- Hereditary Ovarian Carcinoma [NCIt concept]
- Hereditary Pancreatic Carcinoma [NCIt concept]
- Hereditary Papillary Renal Cell Carcinoma [NCIt concept]
- Hereditary Paraganglioma [NCIt concept]
- Hereditary Paraganglioma-Pheochromocytoma Syndrome [NCIt concept]
- Hereditary Prostate Carcinoma [NCIt concept]
- Hereditary Pyropoikilocytosis [NCIt concept]
- Hereditary Renal Cell Carcinoma [NCIt concept]
- Hereditary Retinal Dystrophy [NCIt concept]
- Hereditary Retinoblastoma [NCIt concept]
- Hereditary Sideroblastic Anemia [NCIt concept]
- Hereditary Spherocytosis [NCIt concept]
- Hereditary Thyroid Gland Medullary Carcinoma [NCIt concept]
- Hereditary Tumor Syndrome Associated with Homologous Recombination Pathway Mutations [NCIt concept]
- Hyperparathyroidism-Jaw Tumor Syndrome [NCIt concept]
- Infantile Pyknocytosis [NCIt concept]
- Inherited Bone Marrow Failure Syndrome [NCIt concept]
- Juvenile Myelomonocytic Leukemia Associated with Neurofibromatosis [NCIt concept]
- Juvenile Myelomonocytic Leukemia Associated with Noonan Syndrome-Like Disorder [NCIt concept]
- Juvenile Polyposis Syndrome [NCIt concept]
- LZTR1 Schwannomatosis 2 [NCIt concept]
- Leber Hereditary Optic Atrophy [NCIt concept]
- Li-Fraumeni Syndrome [NCIt concept]
- Lynch 1 Syndrome [NCIt concept]
- Lynch 2 Syndrome [NCIt concept]
- Lynch Syndrome [NCIt concept]
- MAFA Related Familial Insulinomatosis [NCIt concept]
- MUTYH-Associated Polyposis [NCIt concept]
- Meesmann Corneal Dystrophy [NCIt concept]
- Melanoma-Astrocytoma Syndrome [NCIt concept]
- Melanoma-Pancreatic Cancer Syndrome [NCIt concept]
- Metastatic BRCA-Associated Breast Carcinoma [NCIt concept]
- Monosomy 7 Myelodysplasia and Leukemia Syndrome 1 [NCIt concept]
- Multiple Self Healing Epithelioma of Ferguson-Smith [NCIt concept]
- Myeloid Leukemia Associated with Down Syndrome [NCIt concept]
- Neurofibromatosis [NCIt concept]
- Neurofibromatosis Type 1 [NCIt concept]
- Neurofibromatosis Type 1 with Inoperable, Progressive, Symptomatic Plexiform Neurofibromas [NCIt concept]
- Neurofibromatosis Type 2 [NCIt concept]
- Nevoid Basal Cell Carcinoma Syndrome [NCIt concept]
- Noonan Syndrome-Like Disorder [NCIt concept]
- Optic Atrophy 1 [NCIt concept]
- PALB2-Associated Breast Carcinoma [NCIt concept]
- PALB2-Associated Malignant Neoplasm [NCIt concept]
- PTEN Hamartoma Tumor Syndrome [NCIt concept]
- Peutz-Jeghers Syndrome [NCIt concept]
- Phakomatosis [NCIt concept]
- Polymerase Proofreading Associated Polyposis [NCIt concept]
- Proteus-Like Syndrome [NCIt concept]
- Pyrimidine-5'-Nucleotidase Deficiency [NCIt concept]
- Recurrent BRCA- Associated Ovarian Carcinoma [NCIt concept]
- Recurrent Hereditary Thyroid Gland Medullary Carcinoma [NCIt concept]
- Recurrent Neurofibromatosis Type 1 [NCIt concept]
- Refractory Neurofibromatosis Type 1 [NCIt concept]
- Renal Cell Carcinoma with Constitutional Chromosome 3 Translocations [NCIt concept]
- Retinal Cone Dystrophy 3B [NCIt concept]
- Retinal Dystrophy with Inner Retinal Dysfunction and Ganglion Cell Abnormalities [NCIt concept]
- Retinal Dystrophy with or without Extraocular Anomalies [NCIt concept]
- Rhabdoid Tumor Predisposition Syndrome [NCIt concept]
- Rhabdoid Tumor Predisposition Syndrome 1 [NCIt concept]
- Rhabdoid Tumor Predisposition Syndrome 2 [NCIt concept]
- Roberts-SC Phocomelia Syndrome [NCIt concept]
- Rothmund-Thomson Syndrome [NCIt concept]
- Rothmund-Thomson Syndrome Type 1 [NCIt concept]
- Rothmund-Thomson Syndrome Type 2 [NCIt concept]
- SAMD9-Associated Hereditary Myelodysplastic Syndrome [NCIt concept]
- SAMD9L-Associated Hereditary Myelodysplastic Syndrome [NCIt concept]
- SMARCB1 Schwannomatosis 1 [NCIt concept]
- Schwannomatosis [NCIt concept]
- Short Limb Dwarfism-Saddle Nose-Spinal Alterations-Metaphyseal Striation Syndrome [NCIt concept]
- Shwachman-Diamond Syndrome [NCIt concept]
- Sturge-Weber Syndrome [NCIt concept]
- Succinate Dehydrogenase-Deficient Tumor Syndrome [NCIt concept]
- TP53-Associated Li-Fraumeni Syndrome [NCIt concept]
- Transient Abnormal Myelopoiesis Associated with Down Syndrome [NCIt concept]
- Triosephosphate Isomerase Deficiency [NCIt concept]
- Tuberous Sclerosis [NCIt concept]
- Tuberous Sclerosis 1 [NCIt concept]
- Tuberous Sclerosis 2 [NCIt concept]
- Turcot Syndrome [NCIt concept]
- Turcot Syndrome Type 1 [NCIt concept]
- Turcot Syndrome Type 2 [NCIt concept]
- Unresectable Hereditary Thyroid Gland Medullary Carcinoma [NCIt concept]
- Von Hippel Lindau Syndrome [NCIt concept]
- WAGR Syndrome [NCIt concept]
- Werner Syndrome [NCIt concept]
- Wilms Tumor-Aniridia-Genitourinary Anomalies-Mental Retardation-Obesity Syndrome [NCIt concept]
- Wiskott-Aldrich Syndrome [NCIt concept]
- X-Linked Agammaglobulinemia [NCIt concept]
is_not_finding_of_disease
- Acute Myeloid Leukemia with Biallelic CEBPA Mutation [NCIt concept]
- Acute Myeloid Leukemia with CEBPA Mutation [NCIt concept]
- Acute Myeloid Leukemia with Monoallelic CEBPA Mutation [NCIt concept]
- Bilateral Synchronous Sporadic Renal Cell Carcinoma [NCIt concept]

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