Phenotypes for disease #01074 (OKS (Opitz-Kaveggia syndrome (OKS)), OMIM:305450)

10 entries on 1 page. Showing entries 1 - 10.
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Phenotype details     

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Age/Examination     

Age/Diagnosis     

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0000060421 Opitz-Kaveggia syndrome (OMIM:305450) - - Familial, X-linked - - - - - Daniel Trujillano 00080852
0000204037 see paper; … Opitz-Kaveggia syndrome OKS Familial, X-linked recessive - - - - - Johan den Dunnen 00266262
0000204038 see paper; … Opitz-Kaveggia syndrome OKS Familial, X-linked recessive - - - - - Johan den Dunnen 00266263
0000204039 see paper; … Opitz-Kaveggia syndrome OKS Familial, X-linked recessive - - - - - Johan den Dunnen 00266264
0000204040 see paper; …, mental retardation, macrocephaly, imperforate anus, hypotonia Opitz-Kaveggia syndrome OKS Familial, X-linked recessive - - - - - Johan den Dunnen 00266265
0000204041 see paper; … Opitz-Kaveggia syndrome OKS Familial, X-linked recessive - - - - - Johan den Dunnen 00266266
0000204042 see paper; … Opitz-Kaveggia syndrome OKS Familial, X-linked recessive - - - - - Johan den Dunnen 00266267
0000204043 see paper; … Opitz-Kaveggia syndrome OKS Familial, X-linked recessive - - - - - Johan den Dunnen 00266268
0000204044 see paper; … Opitz-Kaveggia syndrome OKS Familial, X-linked recessive - - - - - Johan den Dunnen 00266269
0000334618 Neurodevelopmental delay, Abnormal facial shape, Wide anterior fontanel, Microcephaly, Failure to thrive, Micropenis - - Isolated (sporadic) 01y - - - - Andreas Laner 00445383
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