Phenotypes for disease #05769 (KLEFS1 (Kleefstra syndrome, type 1 (KLEFS1)), OMIM:610253)

5 entries on 1 page. Showing entries 1 - 5.
Legend   How to query  

AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Owner     

Individual ID     
0000243176 - - (+) 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 Unknown - 20y - - Andreas Laner 00324676
0000246780 - - (+) Hearing abnormality,(+) Hearing impairment,(+) Delayed speech and language development,(+) Global developmental delay,(+) Absent speech,(+) Neurological speech impairment,(+) Neurodevelopmental delay ; sister also affected, not tested Unknown 01y - - - Andreas Laner 00328552
0000252692 - - 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, Unknown 04y - - - Andreas Laner 00334943
0000303948 - - Microcephaly, Short attention span, Delayed speech and language development, Global developmental delay, Plagiocephaly Isolated (sporadic) 02y - - - Andreas Laner 00411922
0000325532 - - Hypotonia, Motor delay,Joint hypermobility,High hypermetropia,Neurodevelopmental delay, Pectus excavatum, Behavioral problems Isolated (sporadic) 02y - - - Andreas Laner 00435335
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.