Disease #05769 (KLEFS1 (Kleefstra syndrome, type 1 (KLEFS1)), OMIM:610253)

Official abbreviation KLEFS1
Name Kleefstra syndrome, type 1 (KLEFS1)
OMIM ID 610253
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 12
Phenotype entries for this disease 5
Associated with 1 gene EHMT1
Associated tissues -
Disease features -
Remarks -
Date created 2020-06-12 11:38:53 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

12 entries on 1 page. Showing entries 1 - 12.
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00324676 169067 - - M ? Germany - - - - - KLEFS1 (+) Abnormality of the nervous system,(+) Behavioral abnormality,(+) Intellectual disability,(+) Seizure,(+) Abnormality of higher mental function,(+) Abnormal nervous system physiology,(+) Abnormal nervous system morphology,(+) Neurodevelopmental abnormality,(+) Diminished ability to concentrate EHMT1 EHMT1 1 1 Andreas Laner
00328552 175109 - - M ? Germany - - - - - KLEFS1 (+) Hearing abnormality,(+) Hearing impairment,(+) Delayed speech and language development,(+) Global developmental delay,(+) Absent speech,(+) Neurological speech impairment,(+) Neurodevelopmental delay ; sister also affected, not tested EHMT1 EHMT1 1 1 Andreas Laner
00334943 161151 - - M ? Germany - - - - - KLEFS1 Clinical suspicion of Sotos syndrome, tall, overweight, facial dysmorphia (large long head, large forehead, epicanthus, puffy tent-like lips, small teeth with gaps). Rather clumsy large hands, no weakness in drinking as a baby, EHMT1 EHMT1 1 1 Andreas Laner
00373344 - - - - no China - - - - - KLEFS1 - - EHMT1 1 1 Ke Xu
00373345 - - - F no China - - - - - KLEFS1 - - EHMT1 1 1 Ke Xu
00373346 - - - F no China - - - - - KLEFS1 - - EHMT1 1 1 Ke Xu
00373347 - - - M no - - - - - - KLEFS1 - - EHMT1 1 1 Ke Xu
00373348 - - - F no China - - - - - KLEFS1 - - EHMT1 1 1 Ke Xu
00373349 - - - M no China - - - - - KLEFS1 - - EHMT1 1 1 Ke Xu
00373350 - - - M no China - - - - - KLEFS1 - - EHMT1 1 1 Ke Xu
00411922 199204 - - M ? Turkey - - - - - KLEFS1 Microcephaly, Short attention span, Delayed speech and language development, Global developmental delay, Plagiocephaly EHMT1 EHMT1 1 1 Andreas Laner
00435335 263280 - - F no Germany - - - - - KLEFS1 Hypotonia, Motor delay,Joint hypermobility,High hypermetropia,Neurodevelopmental delay, Pectus excavatum, Behavioral problems EHMT1 EHMT1 1 1 Andreas Laner
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