DiseaseID 17205

琥珀酰辅酶A连接酶缺乏症

disease

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Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.

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Disease: 1Symptom: 12Target: 3Links: 15
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Record Fields

Scalar fields from the final disease record.

Disease Id
17205
Core Entity Id
75397
Source Entity Count
1
Preferred Name
Succinate-Coa Ligase Deficiency
Name Cn
琥珀酰辅酶A连接酶缺乏症
Name Pinyin
Hu Po Xian Fu Mei A Lian Jie Mei Que Fa Zheng
Name En
Succinate-Coa Ligase Deficiency
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Nervous System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal DiseasesNutritional and Metabolic Diseases
Do Class
genetic disease; disease of metabolism
Hpo Class
Mesh Class Name
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System DiseasesNutritional and Metabolic Diseases
Hpo Class Name
Do Class Name
disease of metabolism; genetic disease
Disease Definition
Version
v1,v2
Suppressed
No

Names

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

Name
Succinate-Coa Ligase Deficiency
Role
preferred
Name
Mitochondrial Dna Depletion Syndrome 9 (Encephalomyopathic Type With Methylmalonic Aciduria)
Role
preferred
Name
MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)
Role
preferred
Name
Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form, With Methylmalonic Aciduria, Autosomal Recessive
Role
preferred
Name
LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY
Role
alias
Name
MTDPS9
Role
alias
Name
Mitochondrial Dna Depletion Syndrome 5
Role
alias
Name
Mitochondrial Dna Depletion Syndrome 9
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS019819HBDIS020834HBDIS021543HBDIS022056
Omim
245400612073
Umls
C2749864C3151476
Sym Map
SMDE02353SMDE04878
Do Class
DOID:0014667DOID:630
Dis Ge Net
C2749864C3151476C3501372C3711369
Umls Sty
T047
Me Sh Class
C05C10C16C18
Tcmbank Disease
2139123577249333712

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Do Class Name
disease of metabolism; genetic disease
Disease Type
disease
Do Disease Class
genetic disease; disease of metabolism
Umls Disease Type
Disease or Syndrome
Me Sh Disease Class
Nervous System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal DiseasesNutritional and Metabolic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System DiseasesNutritional and Metabolic Diseases
Umls Semantic Type Name
Disease or Syndrome