DiseaseID 5081
视网膜母细胞瘤
disease
NCI2016_02D:A benign or malignant neoplasm affecting the retina. Representative examples of benign neoplasms include retinocytoma and hemangioma. Representative examples of malignant neoplasms include retinoblastoma, lym
Relationship Network
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Disease: 1Experiment: 1Symptom: 10Target: 12Links: 23
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 5081
- Core Entity Id
- 61525
- Source Entity Count
- 1
- Preferred Name
- Retinoblastoma
- Name Cn
- 视网膜母细胞瘤
- Name Pinyin
- Shi Wang Mo Mu Xi Bao Liu
- Name En
- Retinoblastoma
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Neoplastic Process
- Disgenet Type
- disease
- Mesh Class
- Eye Diseases; Neoplasms
- Do Class
- disease of anatomical entity; disease of cellular proliferation
- Hpo Class
- Abnormality of the eye; Neoplasm
- Mesh Class Name
- Neoplasms; Eye Diseases
- Hpo Class Name
- Neoplasm; Abnormality of the eye
- Do Class Name
- disease of anatomical entity; disease of cellular proliferation
- Disease Definition
- NCI2016_02D:A benign or malignant neoplasm affecting the retina. Representative examples of benign neoplasms include retinocytoma and hemangioma. Representative examples of malignant neoplasms include retinoblastoma, lymphoma and melanoma.|MSH2017_2016_08_12:Tumors or cancer of the RETINA.|HPO2016_07_04:A tumor (abnormal growth of tissue) of the retina. [CINEAS:asollie]
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Retinoblastoma
Role
preferred
Name
Retinal Neoplasms
Role
preferred
Name
Familial Retinoblastoma
Role
preferred
Name
Malignant Neoplasm of Retina
Role
preferred
Name
Sporadic Retinoblastoma
Role
preferred
Name
Cancer of The Retina
Role
alias
Name
RB
Role
alias
Name
RB1
Role
alias
Name
Retina
Role
alias
Name
Retina Tumor
Role
alias
Name
Retinal Cancer
Role
alias
Name
Retinal Neoplasm
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0009919HP:0012777
Herb
HBDIS001843HBDIS002625HBDIS009978HBDIS011320HBDIS011321
Me Sh
D012175D019572
Omim
180200
Umls
C0035335C0524801
Icd10
C69.2
Sym Map
SMDE01210SMDE12837
Do Class
DOID:14566DOID:7
Dis Ge Net
C0024622C0035335C0524801C0751483C0751484
Umls Sty
T191
Hpo Class
HP:0000478HP:0002664
Me Sh Class
C04C11
Tcmbank Disease
11272160261773323561237712547
Itcmdb Generated
ITX-DISEASE-460CE837EDDCITX-DISEASE-ACE53E2D8721
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2v2
Suppress
0
Do Class Name
disease of anatomical entity; disease of cellular proliferation
Disease Type
diseasegroup
Hpo Class Name
Neoplasm; Abnormality of the eye
Do Disease Class
disease of anatomical entity; disease of cellular proliferation
Hpo Disease Class
Abnormality of the eye; Neoplasm
Umls Disease Type
Neoplastic Process
Disease Definition
NCI2016_02D:A benign or malignant neoplasm affecting the retina. Representative examples of benign neoplasms include retinocytoma and hemangioma. Representative examples of malignant neoplasms include retinoblastoma, lymphoma and melanoma.|MSH2017_2016_08_12:Tumors or cancer of the RETINA.|HPO2016_07_04:A tumor (abnormal growth of tissue) of the retina. [CINEAS:asollie]NCI2016_NICHD_1602D:A malignant tumor of the eye comprised of immature retinal cells.|NCI2016_NCI-GLOSS_1602D:Cancer that forms in the tissues of the retina (the light-sensitive layers of nerve tissue at the back of the eye). Retinoblastoma usually occurs in children younger than 5 years. It may be hereditary or nonhereditary (sporadic).|NCI2016_CDISC_1602D:A malignant neoplasm originating in the nuclear layer of the retina.|NCI2016_02D:A neuroblastoma arising from the retina.|NCI2016_02D:A malignant tumor that originates in the nuclear layer of the retina. As the most common primary tumor of the eye in children, retinoblastoma is still relatively uncommon, accounting for only 1% of all malignant tumors in pediatric patients. Approximately 95% of cases are diagnosed before age 5. These tumors may be multifocal, bilateral, congenital, inherited, or acquired. Seventy-five percent of retinoblastomas are unilateral; 60% occur sporadically. A predisposition to retinoblastoma has been associated with 13q14 cytogenetic abnormalities. Patients with the inherited form also appear to be at increased risk for secondary nonocular malignancies such as osteosarcoma, malignant fibrous histiocytoma, and fibrosarcoma.|MSH2017_2016_08_12:A malignant tumor arising from the nuclear layer of the retina that is the most common primary tumor of the eye in children. The tumor tends to occur in early childhood or infancy and may be present at birth. The majority are sporadic, but the condition may be transmitted as an autosomal dominant trait. Histologic features include dense cellularity, small round polygonal cells, and areas of calcification and necrosis. An abnormal pupil reflex (leukokoria); NYSTAGMUS, PATHOLOGIC; STRABISMUS; and visual loss represent common clinical characteristics of this condition. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2104)|HPO2016_07_04:A tumor of the eye originating from cells of the retina. [HPO:curators]|CSP2006:malignant congenital blastoma, occurring in both hereditary and sporadic forms, composed of tumor cells arising from the retinoblasts; the most common tumor of the eye in children.
Me Sh Disease Class
Eye Diseases; Neoplasms
Dis Ge Net Disease Type
diseasegroup
Disease Class Name Me Sh
Neoplasms; Eye Diseases
Umls Semantic Type Name
Neoplastic Process