DiseaseID 16205
尺骨-乳腺综合征
disease
SNOMEDCT_US_2016_09_01:An extremely rare inherited disorder characterized by malformations of the ulnar ray, hypoplasia and dysfunction of the axillary apocrine and mammary glands, endocrine dysfunction, dental anomalies
Relationship Network
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Disease: 1Symptom: 2Target: 7Links: 9
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 16205
- Core Entity Id
- 74242
- Source Entity Count
- 1
- Preferred Name
- Ulnar-Mammary Syndrome
- Name Cn
- 尺骨-乳腺综合征
- Name Pinyin
- Chi Gu - Ru Xian Zong He Zheng
- Name En
- Ulnar-Mammary Syndrome
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Do Class
- syndrome; genetic disease
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
- Hpo Class Name
- Do Class Name
- genetic disease; syndrome
- Disease Definition
- SNOMEDCT_US_2016_09_01:An extremely rare inherited disorder characterized by malformations of the ulnar ray, hypoplasia and dysfunction of the axillary apocrine and mammary glands, endocrine dysfunction, dental anomalies, and occasional visceral malformations.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Ulnar-Mammary Syndrome
Role
preferred
Name
PALLISTER ULNAR-MAMMARY SYNDROME
Role
alias
Name
SCHINZEL SYNDROME
Role
alias
Name
UMS
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS018349
Omim
181450
Umls
C1866994
Sym Map
SMDE02665
Do Class
DOID:225DOID:630
Dis Ge Net
C1866994
Umls Sty
T047
Me Sh Class
C16C17
Tcmbank Disease
5079
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Do Class Name
genetic disease; syndrome
Disease Type
disease
Do Disease Class
syndrome; genetic disease
Umls Disease Type
Disease or Syndrome
Disease Definition
SNOMEDCT_US_2016_09_01:An extremely rare inherited disorder characterized by malformations of the ulnar ray, hypoplasia and dysfunction of the axillary apocrine and mammary glands, endocrine dysfunction, dental anomalies, and occasional visceral malformations.
Me Sh Disease Class
Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
Umls Semantic Type Name
Disease or Syndrome