Breast carcinoma
Symptom Information:
Symptom ID: | HPO:0003002 | |||||||||||||||||||||||||||||||||||
Synonyms: |
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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) Neoplasm by anatomical site(HPO:0011793) Neoplasm of the breast(HPO:0100013) Breast carcinoma(HPO:0003002) Abnormality of the breast(HPO:0000769) Neoplasm of the breast(HPO:0100013) Breast carcinoma(HPO:0003002) MedDRA: Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104) Breast neoplasms malignant and unspecified (incl nipple)(MedDRA:10006291) Breast and nipple neoplasms malignant(MedDRA:10006290) Breast carcinoma(HPO:0003002) |
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Database Frequency: | 23 / 7739 | |||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
APOCRINE GLAND SECRETION, VARIATION IN | (OMIM:117800) |
BREAST CANCER | (OMIM:114480) |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 | (OMIM:604370) |
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2 | (OMIM:612555) |
COWDEN SYNDROME 2 | (OMIM:612359) |
COWDEN SYNDROME 5 | (OMIM:615108) |
COWDEN SYNDROME 6 | (OMIM:615109) |
Carney complex | (Orphanet:1359) |
Cowden syndrome | (Orphanet:201) |
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome | (Orphanet:313846) |
Hereditary breast and ovarian cancer syndrome | (Orphanet:145) |
Hereditary breast cancer | (Orphanet:227535) |
Insulin-resistance syndrome type A | (Orphanet:2297) |
LI-FRAUMENI SYNDROME 1 | (OMIM:151623) |
LI-FRAUMENI SYNDROME 2 | (OMIM:609265) |
Lhermitte-Duclos disease | (Orphanet:65285) |
Li-Fraumeni syndrome | (Orphanet:524) |
Muir-Torre syndrome | (Orphanet:587) |
OVARIAN CANCEROVARIAN CANCER, EPITHELIAL, INCLUDED | (OMIM:167000) |
Peutz-Jeghers syndrome | (Orphanet:2869) |
Proteus-like syndrome | (Orphanet:2969) |
Saethre-Chotzen syndrome | (Orphanet:794) |
Werner syndrome | (Orphanet:902) |