DiseaseID 947

Meier-Gorlin综合征1型

disease

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Disease: 1Formula: 20Symptom: 5Target: 23Links: 49
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Record Fields

Scalar fields from the final disease record.

Disease Id
947
Core Entity Id
1071
Source Entity Count
1
Preferred Name
Meier-Gorlin Syndrome 1
Name Cn
Meier-Gorlin综合征1型
Name Pinyin
Meier-gorlin Zong He Zheng 1 Xing
Name En
Meier-Gorlin Syndrome 1
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Stomatognathic Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Pathological Conditions, Signs and Symptoms; Otorhinolaryngologic Diseases; Musculoskeletal Diseases
Do Class
syndrome; genetic disease
Hpo Class
Mesh Class Name
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases
Hpo Class Name
Do Class Name
genetic disease; syndrome
Disease Definition
Version
v1,v2
Suppressed
No

Names

Preferred names, aliases, and source labels retained in the final schema.

Name
Meier-Gorlin Syndrome 1
Role
preferred
Name
EAR, PATELLA, SHORT STATURE SYNDROME
Role
preferred
Name
EPS
Role
alias
Name
MEIER-GORLIN SYNDROME
Role
alias
Name
MGORS1
Role
alias
Name
MICROTIA, ABSENT PATELLAE, MICROGNATHIA SYNDROME
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS018474HBDIS027383
Omim
224690
Umls
C1868684
Sym Map
SMDE00316
Do Class
DOID:225DOID:630
Dis Ge Net
C1868684C4552001
Umls Sty
T047
Me Sh Class
C05C07C09C16C23
Etcm Disease
Meier-Gorlin Syndrome 1
Tcmbank Disease
1126411354
Itcmdb Generated
ITX-DISEASE-CE0453F49D66

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Page Title
Disease Meier-Gorlin Syndrome 1 Details page
Do Class Name
genetic disease; syndrome
Disease Type
disease
Do Disease Class
syndrome; genetic disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Meier-Gorlin Syndrome 1
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Bone diseases;Neuronal diseases
Me Sh Disease Class
Stomatognathic Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Pathological Conditions, Signs and Symptoms; Otorhinolaryngologic Diseases; Musculoskeletal Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases
Umls Semantic Type Name
Disease or Syndrome