Disease #00064 (CLN1 (lipofuscinosis, ceroid, neuronal, type 1 (CLN-1)), OMIM:256730)

Official abbreviation CLN1
Name lipofuscinosis, ceroid, neuronal, type 1 (CLN-1)
OMIM ID 256730
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 8
Phenotype entries for this disease 9
Associated with 1 gene PPT1
Associated tissues -
Disease features -
Remarks -
Date created 2012-10-23 09:54:48 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

8 entries on 1 page. Showing entries 1 - 8.
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00307853 ? - - F yes Uzbekistan - - - - - CLN1 EEG abnormality, Leukodystrophy, Abnormality of the periventricular white matter PPT1 PPT1 1 1 Corina-Marcela Rus
00307854 ? - - M yes Egypt - - - - - CLN1 Optic disc pallor, Delayed speech and language development, Muscular hypotonia, Dystonia, Cerebral cortical atrophy, Exaggerated startle response, Developmental regression, Myoclonic spasms, Brain atrophy, Abnormality of movement PPT1 PPT1 1 1 Corina-Marcela Rus
00307855 ? - - F ? India - - - - - CLN1 - PPT1 PPT1 1 1 Corina-Marcela Rus
00307856 ? - - M yes Saudi Arabia - - - - - CLN1 - PPT1 PPT1 1 1 Corina-Marcela Rus
00307857 ? - - F yes Iran - - - - - CLN1 Microcephaly, Motor delay, Frequent falls, Developmental regression, Bruxism PPT1 PPT1 1 1 Corina-Marcela Rus
00307858 ? - - F yes Egypt - - - - - CLN1 Microcephaly, Cerebellar atrophy, Cerebral cortical atrophy, Developmental regression, Brain atrophy PPT1 PPT1 1 1 Corina-Marcela Rus
00307859 ? - - F no Egypt - - - - - CLN1 Microcephaly, Dementia, Cerebellar atrophy, Bulbar palsy, Spastic tetraparesis, Dysphagia, Cerebral atrophy, Generalized myoclonic seizures, Neurodegeneration, Developmental regression, Hyperkinesis, Brain atrophy PPT1 PPT1 1 1 Corina-Marcela Rus
00307872 ? - - M no Turkey - - - - - CLN1 Visual impairment, Delayed speech and language development, Seizures, Global developmental delay, Generalized-onset seizure, Developmental regression PPT1 PPT1 1 1 Corina-Marcela Rus
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