Neoplasm
Symptom Information:
Symptom ID: | HPO:0002664 | |||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||||||||||||||||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Neoplasm(HPO:0002664) MedDRA: Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104) Miscellaneous and site unspecified neoplasms malignant and unspecified(MedDRA:10027655) Neoplasms unspecified malignancy and site unspecified NEC(MedDRA:10029111) Neoplasm(HPO:0002664) |
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Database Frequency: | 111 / 7739 | |||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ACTH-independent macronodular adrenal hyperplasia | (Orphanet:189427) |
AGAMMAGLOBULINEMIA, X-LINKED | (OMIM:300755) |
Aase-Smith syndrome | (Orphanet:916) |
Acquired hypertrichosis lanuginosa | (Orphanet:2221) |
Acquired ichthyosis | (Orphanet:454) |
Adamantinoma | (Orphanet:55881) |
Alpha-thalassemia - myelodysplastic syndrome | (Orphanet:231401) |
Antisynthetase syndrome | (Orphanet:81) |
Ataxia-telangiectasia | (Orphanet:100) |
Autosomal recessive hyper-IgE syndrome | (Orphanet:169446) |
BROOKE-SPIEGLER SYNDROME | (OMIM:605041) |
Bannayan-Riley-Ruvalcaba syndrome | (Orphanet:109) |
Beckwith-Wiedemann syndrome | (Orphanet:116) |
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 | (Orphanet:231117) |
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 | (Orphanet:96193) |
Blackfan-Diamond anemia | (Orphanet:124) |
Bloom syndrome | (Orphanet:125) |
CANCER, FAMILIAL, WITH IN VITRO RADIORESISTANCE | (OMIM:114450) |
CARCINOEMBRYONIC ANTIGEN-RELATED CELL ADHESION MOLECULE 5 | (OMIM:114890) |
CERVICAL CANCER | (OMIM:603956) |
CHROMOSOMAL INSTABILITY WITH TISSUE-SPECIFIC RADIOSENSITIVITY | (OMIM:215510) |
CYCLIN-DEPENDENT KINASE 11B | (OMIM:176873) |
CYTOCHROME P450, SUBFAMILY I, POLYPEPTIDE 1 | (OMIM:108330) |
Carney triad | (Orphanet:139411) |
Cheilitis glandularis | (Orphanet:1221) |
Chylous ascites | (Orphanet:1160) |
Combined immunodeficiency due to CRAC channel dysfunction | (Orphanet:169090) |
Combined immunodeficiency due to DOCK8 deficiency | (Orphanet:217390) |
Complete androgen insensitivity syndrome | (Orphanet:99429) |
Costello syndrome | (Orphanet:3071) |
Cowden syndrome | (Orphanet:201) |
Cronkhite-Canada syndrome | (Orphanet:2930) |
DRUG METABOLISM, POOR, CYP2D6-RELATEDDRUG METABOLISM, ULTRARAPID, CYP2D6-RELATED, INCLUDED | (OMIM:608902) |
Dermatomyositis | (Orphanet:221) |
Dubowitz syndrome | (Orphanet:235) |
Dyskeratosis congenita | (Orphanet:1775) |
Dystrophic epidermolysis bullosa | (Orphanet:303) |
ELK1, MEMBER OF ETS ONCOGENE FAMILY | (OMIM:311040) |
ETS VARIANT GENE 1 | (OMIM:600541) |
Enchondromatosis | (Orphanet:296) |
Epidermolysis bullosa simplex | (Orphanet:304) |
Extramammary Paget disease | (Orphanet:2800) |
Familial adenomatous polyposis | (Orphanet:733) |
Familial keratoacanthoma | (Orphanet:493) |
Familial multiple fibrofolliculoma | (Orphanet:338) |
Fanconi anemia | (Orphanet:84) |
Fetal hydantoin syndrome | (Orphanet:1912) |
Gestational trophoblastic neoplasm | (Orphanet:59305) |
Gorlin syndrome | (Orphanet:377) |
Hairy cell leukemia variant | (Orphanet:300878) |
Hodgkin lymphoma | (Orphanet:98293) |
Hodgkin lymphoma, classical | (Orphanet:391) |
Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
IMMUNODEFICIENCY, COMMON VARIABLE, 2 | (OMIM:240500) |
Inherited epidermolysis bullosa | (Orphanet:79361) |
Intestinal lymphangiectasia | (Orphanet:36204) |
KERATOSIS, FAMILIAL ACTINIC | (OMIM:148390) |
KID syndrome | (Orphanet:477) |
Kaposi's sarcoma | (Orphanet:33276) |
Large congenital melanocytic nevus | (Orphanet:626) |
Li-Fraumeni syndrome | (Orphanet:524) |
Lichen amyloidosis | (Orphanet:49804) |
MCF.2 CELL LINE-DERIVED TRANSFORMING SEQUENCE | (OMIM:311030) |
Malignant peritoneal mesothelioma | (Orphanet:168811) |
Mazabraud syndrome | (Orphanet:57782) |
Megalencephaly-capillary malformation-polymicrogyria syndrome | (Orphanet:60040) |
Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
Multiple endocrine neoplasia type 1 | (Orphanet:652) |
Multiple keratoacanthoma, Ferguson-Smith type | (Orphanet:65748) |
Multiple osteochondromas | (Orphanet:321) |
Myasthenia gravis | (Orphanet:589) |
N syndrome | (Orphanet:2608) |
Nasopharyngeal carcinoma | (Orphanet:150) |
Nephroblastoma | (Orphanet:654) |
Neurocutaneous melanocytosis | (Orphanet:2481) |
Neurofibromatosis type 1 | (Orphanet:636) |
Nijmegen breakage syndrome | (Orphanet:647) |
Nodular lymphocyte predominant Hodgkin lymphoma | (Orphanet:86893) |
ONCOCYTOMA | (OMIM:553000) |
OSLAM syndrome | (Orphanet:2760) |
PHEOCHROMOCYTOMAPHEOCHROMOCYTOMA, SUSCEPTIBILITY TO | (OMIM:171300) |
PREMATURE AGING SYNDROME, OKAMOTO TYPE | (OMIM:601811) |
PROSTATE CANCER, HEREDITARY, 1 | (OMIM:601518) |
PTEN hamartoma tumor syndrome | (Orphanet:306498) |
Palmoplantar keratoderma-esophageal carcinoma syndrome | (Orphanet:2198) |
Palmoplantar keratoderma-sclerodactyly syndrome | (Orphanet:384) |
Papilloma of choroid plexus | (Orphanet:2807) |
Peritoneal cystic mesothelioma | (Orphanet:168816) |
Peutz-Jeghers syndrome | (Orphanet:2869) |
Piebaldism | (Orphanet:2884) |
Pityriasis rubra pilaris | (Orphanet:2897) |
Placental site trophoblastic tumor | (Orphanet:99928) |
Primary peritoneal carcinoma | (Orphanet:168829) |
Progressive familial intrahepatic cholestasis | (Orphanet:172) |
Rombo syndrome | (Orphanet:3110) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
Schinzel-Giedion syndrome | (Orphanet:798) |
Secondary intestinal lymphangiectasia | (Orphanet:90363) |
Short stature - deafness - neutrophil dysfunction - dysmorphism | (Orphanet:2866) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
Sotos syndrome | (Orphanet:821) |
Syndromic X-linked ichthyosis | (Orphanet:281090) |
TUMOR NECROSIS FACTOR | (OMIM:191160) |
UV-sensitive syndrome | (Orphanet:178338) |
Von Hippel-Lindau disease | (Orphanet:892) |
Werner syndrome | (Orphanet:902) |
Wiskott-Aldrich syndrome | (Orphanet:906) |
XG REGULATOR | (OMIM:489500) |
Xeroderma pigmentosum | (Orphanet:910) |
Yellow nail syndrome | (Orphanet:662) |
ZINC FINGER PROTEIN 35 | (OMIM:194533) |