DiseaseID 26348
胰岛素样生长因子I抵抗
Insulin-Like Growth Factor I, Resistance To
SNOMEDCT_US_2016_09_01:Variable intrauterine and postnatal growth retardation and elevated serum IGF-I levels. Additional features include variable degrees of intellectual deficit, microcephaly and dysmorphism (broad nas
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
Click a node to open it in a new tab
Disease: 1Symptom: 2Target: 12Links: 14
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 26348
- Core Entity Id
- 118916
- Source Entity Count
- 1
- Preferred Name
- Insulin-Like Growth Factor I, Resistance To
- Name Cn
- 胰岛素样生长因子I抵抗
- Name Pinyin
- Yi Dao Su Yang Sheng Zhang Yin Zi I Di Kang
- Name En
- Insulin-Like Growth Factor I, Resistance To
- Name Latin
- Bilingual Status
- complete
- Disease Type
- Umls Disease Type
- Disgenet Type
- Mesh Class
- Do Class
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- Disease Definition
- SNOMEDCT_US_2016_09_01:Variable intrauterine and postnatal growth retardation and elevated serum IGF-I levels. Additional features include variable degrees of intellectual deficit, microcephaly and dysmorphism (broad nasal bridge and tip, smooth philtrum, thin upper and everted lower lips, short fingers, clinodactyly, wide-set nipples and pectus excavatum). Prevalence is unknown, may be caused by a variety of genetic defects.|NCI2016_02D:Tissue unresponsiveness to insulin-like growth factor-I.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Insulin-Like Growth Factor I, Resistance To
Role
preferred
Source
SymMap_v2
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Umls
C1849157C1849158
Sym Map
SMDE03075
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Disease Definition
SNOMEDCT_US_2016_09_01:Variable intrauterine and postnatal growth retardation and elevated serum IGF-I levels. Additional features include variable degrees of intellectual deficit, microcephaly and dysmorphism (broad nasal bridge and tip, smooth philtrum, thin upper and everted lower lips, short fingers, clinodactyly, wide-set nipples and pectus excavatum). Prevalence is unknown, may be caused by a variety of genetic defects.|NCI2016_02D:Tissue unresponsiveness to insulin-like growth factor-I.