Phenotypes for disease #00610 (CDLS1 (Cornelia de Lange syndrome, type 1 (CDLS-1)), OMIM:122470)

5 entries on 1 page. Showing entries 1 - 5.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000232076 - - - Unknown - - - - - Sha Hong 00306228
0000253327 prenatal growth retardation (HP:0001511), postnatal macrocephaly (HP:0005490), abnormal cardiac morphology (HP:0001627) - - Unknown 00y01m - - - - Andreas Laner 00335380
0000274687 - - Cornelia de Lange syndrome Familial, autosomal dominant - - - - - LOVD 00380834
0000284504 intrauterine growth retardation (HP:0001511), Short long bone, Abnormality of long bone morphology, Abnormal appendicular skeleton morphology, Prenatal maternal abnormality, Preeclampsia, Abnormality of prenatal development or birth; no congenital macrocephaly (-HP:0004488); no cleft; abnormality limbs (HP:0040064) - - Isolated (sporadic) 00y04m - - - - Andreas Laner 00391016
0000323702 microcephaly (HP:0000252) Neurodevelopmental delay, Secundum atrial septal defect, Vesicoureteral reflux, Premature birth, Short stature, Esotropia, Myopia; delayed growth (HP:00001510) - - Isolated (sporadic) 02y - - - - Andreas Laner 00433155
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