Neoplasm

Symptom Information:

Symptom ID: HPO:0002664
Synonyms:
Cancer [HPO:0002664]
Neoplasia [HPO:0002664]
Oncological abnormality [HPO:0002664]
Oncology [HPO:0002664]
Neoplasm and tumor [Orphanet:50000]
Neoplasm (morphologic abnormality) [Orphanet:50000]
Neoplasms [Orphanet:50000]
Neoplasms/tumors [Orphanet:50000]
Neoplasm [Orphanet:50000]
Neoplasm [MedDRA:10028980]
Cystoma [MedDRA:10028980]
Epithelioma [MedDRA:10028980]
Neoplasm growth accelerated [MedDRA:10028980]
Neoplasm NOS [MedDRA:10028980]
Neoplasm of uncertain behavior of endocrine glands and nervous system [MedDRA:10028980]
Neoplasm of uncertain behavior of other and unspecified sites and tissues [MedDRA:10028980]
Neoplasm of uncertain behavior of other specified sites [MedDRA:10028980]
Neoplasm of uncertain behavior, site unspecified [MedDRA:10028980]
Neoplasm of uncertain behaviour of endocrine glands and nervous system [MedDRA:10028980]
Neoplasm of uncertain behaviour of other and unspecified sites and tissues [MedDRA:10028980]
Neoplasm of uncertain behaviour of other specified sites [MedDRA:10028980]
Neoplasm of uncertain behaviour, site unspecified [MedDRA:10028980]
Neoplasm of unspecified nature of bone, soft tissue, and skin [MedDRA:10028980]
Neoplasm of unspecified nature of endocrine glands and other parts of nervous system [MedDRA:10028980]
Neoplasm of unspecified nature of other specified sites [MedDRA:10028980]
Neoplasm of unspecified nature, site unspecified [MedDRA:10028980]
Neoplasms of unspecified nature [MedDRA:10028980]
Neoplasm (NOS) [MedDRA:10028980]
Solid tumour [MedDRA:10028980]
Tumour enlargement [MedDRA:10028980]
Tumor enlargement [MedDRA:10028980]
Solid tumor [MedDRA:10028980]
Epithelioma [OMIM:Epithelioma]
Quality:
Cross references:
Orphanet:50000 "Neoplasms/tumors" [Orphanet:50000]
OMIM: "Epithelioma" [OMIM:Epithelioma]
UMLS:C0027651 "Neoplasia" [HPO:0002664]
UMLS:C0027651 "Neoplasms" [Orphanet:50000]
Is a (Direct Parents):
HPO         Phenotypic abnormality
MedDRA Neoplasms unspecified malignancy and site unspecified NEC
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)
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)