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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
肌萎缩侧索硬化症1型
USH2A c.8559-2A>G
囊性纤维化
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中文
罕见病
Agnathia-Otocephaly Complex (AGOTC)
Alias:
Otocephaly
Agnathia-Holoprosencephaly-Situs Inversus Syndrome
Dysgnathia Complex Agnathia-Holoprosencephaly
Holoprosencephaly-Agnathia
Agotc
Dysgnathia Complex
Cervical Auricle
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基础信息
疾病表征
基因 & 突变
靶点药物
疾病模型
文献报道
无颌-颅面骨发育不全症,也称为颅面骨发育不全症,与小眼症、综合症5和MACS综合症有关,症状包括呼吸困难。与无颌-颅面骨发育不全症相关的基因包括PRRX1(成对相关同源框1),其相关通路/超级通路包括胚胎和诱导多能干细胞和特异性标记物和翻译后修饰:GPI锚定蛋白的合成。相关组织包括眼睛和气管,相关表型包括胼胝体发育不全和窄嘴。
Related ID:
MALACARDS:AGN012
OMIM:202650
MESH:C562503
ICD11:1403653959
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
常显
胎儿期
--
27
220
16
AGN012
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available
Gene & Mutation
#
Gene
Function
Score
Mutations
No data available
Related Drugs
Name
CAS Number
Status
Phase
No data available
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available
References Literature
Title
PMID
Journal
Year
IF
No Data Found!
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