Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Formula: 5Herb: 1Target: 16Links: 30
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 14816
- Core Entity Id
- 72660
- Source Entity Count
- 1
- Preferred Name
- Mental Retardation, X-Linked, With Panhypopituitarism
- Name Cn
- X连锁精神发育迟滞伴全垂体功能减退症
- Name Pinyin
- X Lian Suo Jing Shen Fa Yu Chi Zhi Ban Quan Chui Ti Gong Neng Jian Tui Zheng
- Name En
- Mental Retardation, X-Linked, With Panhypopituitarism
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Endocrine System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Musculoskeletal DiseasesMental Disorders; Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Behavior and Behavior Mechanisms; Endocrine System Diseases
- Do Class
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Endocrine System DiseasesPathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Endocrine System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
- Hpo Class Name
- Do Class Name
- Disease Definition
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Mental Retardation, X-Linked, With Panhypopituitarism
Role
preferred
Name
Mental Retardation, X-Linked, With Isolated Growth Hormone Deficiency
Role
preferred
Name
MRGH
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS016431HBDIS019542
Omim
300123
Umls
C1848068C2678223
Sym Map
SMDE02906
Dis Ge Net
C1848068C2678223
Umls Sty
T047
Me Sh Class
C05C10C16C19C23F01F03
Etcm Disease
Mental Retardation, X-Linked, with Panhypopituitarism
Tcmbank Disease
1100917988
Itcmdb Generated
ITX-DISEASE-6549547E9C28ITX-DISEASE-E273CD3B3225
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Page Title
Disease Mental Retardation, X-Linked, with Panhypopituitarism Details page
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Mental Retardation, X-Linked, with Panhypopituitarism
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Endocrine diseases;Mental diseases;Neuronal diseases
Me Sh Disease Class
Endocrine System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Musculoskeletal DiseasesMental Disorders; Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Behavior and Behavior Mechanisms; Endocrine System Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Endocrine System DiseasesPathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Endocrine System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
Umls Semantic Type Name
Disease or Syndrome