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

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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