DiseaseID 17612
垂体细胞瘤
disease
NCI2016_02D:An extremely rare, WHO grade I, circumscribed and slow-growing tumor that arises from the neurohypophysis or infundibulum and described in adults. It is characterized by the presence of elongated, spindle-sha
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Disease: 1Symptom: 5Target: 2Links: 7
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 17612
- Core Entity Id
- 75876
- Source Entity Count
- 1
- Preferred Name
- Pituicytoma
- Name Cn
- 垂体细胞瘤
- Name Pinyin
- Chui Ti Xi Bao Liu
- Name En
- Pituicytoma
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Neoplastic Process
- Disgenet Type
- disease
- Mesh Class
- Do Class
- Hpo Class
- Abnormality of the nervous system; Abnormality of the endocrine system
- Mesh Class Name
- Hpo Class Name
- Abnormality of the endocrine system; Abnormality of the nervous system
- Do Class Name
- Disease Definition
- NCI2016_02D:An extremely rare, WHO grade I, circumscribed and slow-growing tumor that arises from the neurohypophysis or infundibulum and described in adults. It is characterized by the presence of elongated, spindle-shaped neoplastic glial cells that form storiform patterns or interlacing fascicular arrangements. Signs and symptoms include visual disturbances, headache, amenorrhea, and decreased libido.|HPO2016_07_04:A solid, low grade, spindle cell, glial neoplasm of adults that originates in the neurohypophysis or infundibulum. Clinical signs and symptoms include visual disturbance, headache and features of hypopituitarism. Pituicytomas are well-circumscribed, solid masses that can measure up to several centimeters. Histologically, they show a compact architecture consisting of elongate, bipolar spindle cells arranged in interlacing fascicles or assuming a storiform pattern. [DDD:spark, pmid:17618441, pmid:19109577]
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Pituicytoma
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0011754
Herb
HBDIS020536
Umls
C2986550
Sym Map
SMDE12181
Dis Ge Net
C2986550
Umls Sty
T191
Hpo Class
HP:0000707HP:0000818
Tcmbank Disease
6069
Itcmdb Generated
ITX-DISEASE-7903EC738648
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Type
disease
Hpo Class Name
Abnormality of the endocrine system; Abnormality of the nervous system
Hpo Disease Class
Abnormality of the nervous system; Abnormality of the endocrine system
Umls Disease Type
Neoplastic Process
Disease Definition
NCI2016_02D:An extremely rare, WHO grade I, circumscribed and slow-growing tumor that arises from the neurohypophysis or infundibulum and described in adults. It is characterized by the presence of elongated, spindle-shaped neoplastic glial cells that form storiform patterns or interlacing fascicular arrangements. Signs and symptoms include visual disturbances, headache, amenorrhea, and decreased libido.|HPO2016_07_04:A solid, low grade, spindle cell, glial neoplasm of adults that originates in the neurohypophysis or infundibulum. Clinical signs and symptoms include visual disturbance, headache and features of hypopituitarism. Pituicytomas are well-circumscribed, solid masses that can measure up to several centimeters. Histologically, they show a compact architecture consisting of elongate, bipolar spindle cells arranged in interlacing fascicles or assuming a storiform pattern. [DDD:spark, pmid:17618441, pmid:19109577]
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Neoplastic Process