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Cell Model Catalogue
Patient-Derived Cell Lines
Genetically Modified Cell Lines
Search and Filter
Search
Cell Type
- None -
iPSC
no sample
only primary culture
ICD
- None -
E34.8
E71.1
E75.2
F00.
F06.9
F84.0
G35.0
G40.3
G43.8
G71.0
G71.2
G71.3
G93.4
I42.0
I42.1
I42.2
I42.80
I47.2
I48.-
I49.8
I50.3
I51.81
L93.2
Q02
Q04.8
Q21.3
Q23.4
Q87.0
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
Early infantile epileptic encephalopathy
Encephalopathy
Generalised epilepsy with febrile seizure plus
Heart Failure with Preserved Ejection Fraction
Hypertrophic cardiomyopathy
Hypertrophic obstructive cardiomyopathy
Hypoplastic left heart syndrome
Kabuki syndrome
Lipid storage disorder
Long QT syndrome 1
Long QT syndrome 2
Long QT syndrome 3
Long QT syndrome 7
Mental disorder
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
Takotsubo 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
hPSCreg Name
Cell Type
ICD Code
Disease
Source
Reprogramming
Grade
UMGi163-A
iPSC
WT
WT
Fibroblasts
Plasmid
Research
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