DiseaseID 19374
新生儿马凡综合征
disease
Neonatal Marfan syndrome is a rare, severe and life-threatening genetic disease, occuring during the neonatal period, characterized by classical Marfan syndrome manifestations in addition to facial dy
Relationship Network
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Disease: 1Symptom: 1Target: 1Links: 2
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 19374
- Core Entity Id
- 77887
- Source Entity Count
- 1
- Preferred Name
- Neonatal Marfan Syndrome
- Name Cn
- 新生儿马凡综合征
- Name Pinyin
- Xin Sheng Er Ma Fan Zong He Zheng
- Name En
- Neonatal Marfan Syndrome
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Cardiovascular Diseases; Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
- Do Class
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases
- Hpo Class Name
- Do Class Name
- Disease Definition
- Neonatal Marfan syndrome is a rare, severe and life-threatening genetic disease, occuring during the neonatal period, characterized by classical Marfan syndrome manifestations in addition to facial dy
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Neonatal Marfan Syndrome
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS023199
Sym Map
SMDE01198
Dis Ge Net
C4016054
Orphanet
284979
Umls Sty
T047
Me Sh Class
C05C14C16C17
Tcmbank Disease
22429
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disease Definition
Neonatal Marfan syndrome is a rare, severe and life-threatening genetic disease, occuring during the neonatal period, characterized by classical Marfan syndrome manifestations in addition to facial dy
Me Sh Disease Class
Cardiovascular Diseases; Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases
Umls Semantic Type Name
Disease or Syndrome