Roifman-Chitayat Syndrome (ROCHIS)

Alias:
Combined Immunodeficiency, Facial Dysmorphism, Optic Nerve Atrophy, Skeletal Anomalies, and Developmental Delay
Combined Immunodeficiency with Faciooculoskeletal Anomalies
Rochis
Combined Immunodeficiency with Facio-Oculo-Skeletal Anomalies
Roifman-Chitayat Syndrome, Digenic
Favorite
基础信息
疾病表征
基因 & 突变
靶点药物
疾病模型
文献报道
Roifman-Chitayat 综合症,又称为联合免疫缺陷、面部畸形、视神经萎缩、骨骼异常和发育迟缓,与联合免疫缺陷和免疫缺陷疾病有关,症状包括肌阵挛发作。与 Roifman-Chitayat 综合症相关的重要基因是 KNSTRN (Kinetochore Localized Astrin (SPAG5) Binding Protein)。附属组织包括骨和T细胞,相关表型为智力障碍和共济失调。
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
新生儿
<1/1000000
2
18
2

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!
微信
信息比对
科研助手
使用教程
回到顶部