DiseaseID 14567

前脑无裂畸形伴胎儿运动不能-运动功能减退序列征

phenotype

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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: 16Links: 24
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Record Fields

Scalar fields from the final disease record.

Disease Id
14567
Core Entity Id
72372
Source Entity Count
1
Preferred Name
Holoprosencephaly With Fetal Akinesia-Hypokinesia Sequence
Name Cn
前脑无裂畸形伴胎儿运动不能-运动功能减退序列征
Name Pinyin
Qian Nao Wu Lie Ji Xing Ban Tai Er Yun Dong Bu Neng - Yun Dong Gong Neng Jian Tui Xu Lie Zheng
Name En
Holoprosencephaly With Fetal Akinesia-Hypokinesia Sequence
Name Latin
Bilingual Status
complete
Disease Type
phenotype
Umls Disease Type
Disease or Syndrome
Disgenet Type
phenotype
Mesh Class
Female Urogenital Diseases and Pregnancy Complications; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
Do Class
Hpo Class
Mesh Class Name
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Nervous System Diseases
Hpo Class Name
Do Class Name
Disease Definition
Version
Suppressed

Names

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

Name
Holoprosencephaly With Fetal Akinesia-Hypokinesia Sequence
Role
preferred
Name
Holoprosencephaly with Fetal Akinesia/hypokinesia Sequence
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS016079
Omim
306990
Dis Ge Net
C1844016
Umls Sty
T047
Me Sh Class
C05C10C13C16C23
Etcm Disease
Holoprosencephaly with Fetal Akinesia/hypokinesia Sequence
Tcmbank Disease
29462
Itcmdb Generated
ITX-DISEASE-E0679B1BAA4C

Attributes

Merged source attributes and domain-specific metadata.

Page Title
Disease Holoprosencephaly with Fetal Akinesia/hypokinesia Sequence Details page
Disease Type
phenotype
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Holoprosencephaly with Fetal Akinesia/hypokinesia Sequence
Global Category
Fetal diseases;Rare diseases
Anatomical Category
Neuronal diseases
Me Sh Disease Class
Female Urogenital Diseases and Pregnancy Complications; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
Dis Ge Net Disease Type
phenotype
Disease Class Name Me Sh
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Nervous System Diseases
Umls Semantic Type Name
Disease or Syndrome