Skip to main content
demo.menoci.io
Toggle navigation
Cell Model Catalogue
Patient-Derived Cell Lines
Genetically Modified Cell Lines
External Cell Lines
SFB1002 - AS Project
Export
Stats
Search and Filter
Search
Cell Type
- None -
iPSC
no sample
only primary culture
ICD
- None -
E34.8
E71.1
F00.
F84.0
G35.0
G40.3
G43.8
G71.0
G71.2
G71.3
I42.0
I42.1
I42.2
I42.80
I47.2
I48.-
I49.8
L93.2
Q02
Q04.8
Q21.3
Q23.4
Q87.1
Q87.8
R00.1
Unknown
WT
Disease
- None -
Alström syndrome
Alternating hemiplegia
Arrhythmogenic right ventricular cardiomyopathy
Atrial fibrillation
Autism
Barth syndrome
Bradycardia
Brugada syndrome
Cardiofaciocutaneous syndrome
Cardiomyopathy after chemotherapy
Catecholaminergic polymorphic ventricular tachycardia
Childhood autism
Dementia in Alzheimer disease
Dilated cardiomyopathy
Generalised epilepsy with febrile seizure plus
Hypertrophic cardiomyopathy
Hypertrophic obstructive cardiomyopathy
Hypoplastic left heart syndrome
Long QT syndrome 1
Long QT syndrome 2
Long QT syndrome 3
Long QT syndrome 7
Microcephaly
Mitochondrial myopathy
Multiple sclerosis
Muscular dystrophy
Neonatal lupus erythematosus
Noonan syndrome
Noonan syndrome with multiple lentigines
Overlap syndrome
Periventricular nodular heterotopia
Peroxisome biogenesis disorder spectrum
Progeroid syndrome
Short QT syndrome
Tetralogy of Fallot
Ventricular tachycardia
Vici syndrome
WT
WT/Relative
X-linked myotubular myopathy
Source
- None -
Blood
Bone Marrow
Fibroblasts
Gingiva
Hair
Myoblasts
Skin
Urine
Reprogramming
- None -
Lentivirus
Plasmid
Retrovirus
Sendai Virus
Unknown
mRNA
Grade
- None -
GMP
Other
Research
Gender
- None -
Male
Female
Unknown
Age
- None -
0-10
10-19
20-29
30-39
40-49
50-59
60-69
70-79
<= 80
Search
Lab ID
iPSC ID
hPSCreg Name
Cell Type
ICD Code
Disease
Source
Reprogramming
Grade
No results.
