DiseaseID 2353

也门聋盲-色素减退综合征

disease

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Relationship Network

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

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Disease: 1Target: 1Links: 1
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
2353
Core Entity Id
2652
Source Entity Count
1
Preferred Name
Yemenite Deaf-Blind Hypopigmentation Syndrome
Name Cn
也门聋盲-色素减退综合征
Name Pinyin
Ye Men Long Mang - Se Su Jian Tui Zong He Zheng
Name En
Yemenite Deaf-Blind Hypopigmentation Syndrome
Name Latin
Bilingual Status
complete
Disease Type
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Eye Diseases; Skin and Connective Tissue Diseases; Pathological Conditions, Signs and Symptoms; Otorhinolaryngologic Diseases
Do Class
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
Disease Definition
Version
Suppressed

Names

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

Name
Yemenite Deaf-Blind Hypopigmentation Syndrome
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS029041
Omim
601706
Dis Ge Net
C1866425
Umls Sty
T047
Me Sh Class
C09C10C11C16C17C23

Attributes

Merged source attributes and domain-specific metadata.

Umls Disease Type
Disease or Syndrome
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Eye Diseases; Skin and Connective Tissue Diseases; Pathological Conditions, Signs and Symptoms; Otorhinolaryngologic Diseases
Dis Ge Net Disease Type
disease