DiseaseID 5106

先天性风疹综合征

disease

Relationship Network

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Disease: 1Symptom: 7Target: 4Links: 11

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Record Fields

Scalar fields from the final disease record.

Disease Id: 5106
Core Entity Id: 61553
Source Entity Count: 1
Preferred Name: Congenital Rubella Syndrome
Name Cn: 先天性风疹综合征
Name Pinyin: Xian Tian Xing Feng Zhen Zong He Zheng
Name En: Congenital Rubella Syndrome
Name Latin
Bilingual Status: complete
Disease Type: disease
Umls Disease Type: Disease or Syndrome
Disgenet Type: disease
Mesh Class: Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Infections
Do Class
Hpo Class
Mesh Class Name: Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Infections
Hpo Class Name
Do Class Name
Disease Definition: NCI2016_NICHD_1602D:A condition, whose clinical manifestations include intrauterine growth restriction, petechial rash, jaundice, generalized lymphadenopathy, hepatosplenomegaly, peripheral pulmonary stenosis, cataracts, and sensorineural deafness, that is caused by fetal exposure to the rubella virus during the first trimester of pregnancy.|NCI2016_02D:A condition, whose clinical manifestations include intrauterine growth restriction, petechial rash, jaundice, generalized lymphadenopathy, hepatosplenomegaly, peripheral pulmonary stenosis, cataracts, and sensorineural deafness, that is caused by fetal exposure to the rubella virus during the first trimester of pregnancy.(NICHD)|MSH2017_2016_08_12:Transplacental infection of the fetus with rubella usually in the first trimester of pregnancy, as a consequence of maternal infection, resulting in various developmental abnormalities in the newborn infant. They include cardiac and ocular lesions, deafness, microcephaly, mental retardation, and generalized growth retardation. (From Dorland, 27th ed)
Version: v2
Suppressed: No

Names

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

Name

Congenital Rubella Syndrome

Role

preferred

Name

Rubella Syndrome, Congenital

Role

alias

Cross References

Trusted external identifiers retained for this final record.

Herb

HBDIS002658

Me Sh

D012410

Umls

C0035921

Icd10

P35.0

Sym Map

SMDE07487

Dis Ge Net

C0035921

Umls Sty

T047

Me Sh Class

C01C16

Tcmbank Disease

7445

Attributes

Merged source attributes and domain-specific metadata.

Version

Suppress

Disease Type

disease

Umls Disease Type

Disease or Syndrome

Disease Definition

NCI2016_NICHD_1602D:A condition, whose clinical manifestations include intrauterine growth restriction, petechial rash, jaundice, generalized lymphadenopathy, hepatosplenomegaly, peripheral pulmonary stenosis, cataracts, and sensorineural deafness, that is caused by fetal exposure to the rubella virus during the first trimester of pregnancy.|NCI2016_02D:A condition, whose clinical manifestations include intrauterine growth restriction, petechial rash, jaundice, generalized lymphadenopathy, hepatosplenomegaly, peripheral pulmonary stenosis, cataracts, and sensorineural deafness, that is caused by fetal exposure to the rubella virus during the first trimester of pregnancy.(NICHD)|MSH2017_2016_08_12:Transplacental infection of the fetus with rubella usually in the first trimester of pregnancy, as a consequence of maternal infection, resulting in various developmental abnormalities in the newborn infant. They include cardiac and ocular lesions, deafness, microcephaly, mental retardation, and generalized growth retardation. (From Dorland, 27th ed)

Me Sh Disease Class

Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Infections

Dis Ge Net Disease Type

disease

Disease Class Name Me Sh

Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Infections

Umls Semantic Type Name

Disease or Syndrome