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

4 entries on 1 page. Showing entries 1 - 4.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Growth     

Head/Size     

MotorSkills     

Speech     

Cleft     

Protein     

Abnormality     

Hirsutism     

Intellectual_dis     

Owner     

Individual ID     
0000232076 - - - Unknown - - - - - - - - - - - - - Sha Hong 00306228
0000253327 - 1month - Unknown - - - - retardation prenatal macrocephaly postnatal - - ? - heart - n/a Andreas Laner 00335380
0000274687 - - Cornelia de Lange syndrome Familial, autosomal dominant - - - - - - - - - - - - - LOVD 00380834
0000284504 Intrauterine growth retardation, Short long bone, Abnormality of long bone morphology, Abnormal appendicular skeleton morphology, Prenatal maternal abnormality, Preeclampsia, Abnormality of prenatal development or birth 04mo - Isolated (sporadic) - - - - retardation prenatal no macrocephaly congenital - ? - - limbs ? ? Andreas Laner 00391016
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