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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
Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome (MCAP)
Alias:
Megalencephaly-Capillary Malformation Syndrome
Mcmtc
Mcap
Mcm
Macrocephaly-Capillary Malformation Syndrome
Macrocephaly-Capillary Malformation
Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic
Megalencephaly-Cutis Marmorata Telangiectatica Congenita Syndrome
Macrocephaly-Cutis Marmorata Telangiectatica Congenita Syndrome
Megalencephaly-Cutis Marmorata Telangiectatica Congenita
Megalencephaly Cutis Marmorata Telangiectatica Congenita
Macrocephaly-Cutis Marmorata Telangiectatica Congenita
Macrocephaly Cutis Marmorata Telangiectatica Congenita
M-Cm
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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
巨脑-毛细血管畸形-多小脑回畸形综合征,也称为巨脑-毛细血管畸形综合征,与巨脑和半巨脑有关,症状包括癫痫发作。与巨脑-毛细血管畸形-多小脑回畸形综合征相关的重要基因是PIK3CA(磷脂酰肌醇-4,5-二磷酸3-激酶催化亚基α),其相关通路/超级通路包括信号转导和PIP3激活AKT信号通路。相关组织包括皮肤和大脑,相关表型为巨脑和动静脉畸形。
Related ID:
MALACARDS:MGL038
OMIM:602501
MESH:D013684
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
胎儿期
<1/1000000
4
44
38
MGL038
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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