Phenotypes for disease #05450 (OZEMA;OOMD (ocyte/zygote/embryo maturation arrest))

40 entries on 1 page. Showing entries 1 - 40.
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AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000130177 oocyte maturation defect OOMD-1 see paper; ... Familial, autosomal recessive - - - - - Johan den Dunnen 00165313
0000130178 empty follicle syndrome OOMD-3 see paper; ..., Familial, autosomal dominant - - - - - Johan den Dunnen 00165314
0000130179 empty follicle syndrome OOMD-3 see paper; ... Familial, autosomal dominant - - - - - Johan den Dunnen 00165315
0000130180 empty follicle syndrome OOMD-3 see paper; ... Isolated (sporadic) - - - - - Johan den Dunnen 00165316
0000130181 empty follicle syndrome OOMD-3 - Isolated (sporadic) - - - - - Johan den Dunnen 00165317
0000132933 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168068
0000132944 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168080
0000132945 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168081
0000132946 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168082
0000132947 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168083
0000132948 - - - Familial, autosomal recessive - - - - - Wang Wenjing 00168084
0000132950 - - - Unknown - - - - - Wang Wenjing 00168086
0000132951 - - - Familial, autosomal recessive - - - - - Wang Wenjing 00168087
0000132952 - - - Familial, autosomal recessive - - - - - Wang Wenjing 00168088
0000132953 - - - Familial, autosomal recessive - - - - - Wang Wenjing 00168089
0000132954 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168090
0000132955 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168091
0000132956 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168092
0000132958 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168094
0000132959 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168095
0000132960 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168095
0000132961 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168095
0000132962 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168096
0000132963 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168097
0000132964 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168098
0000132965 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168099
0000132966 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168100
0000132967 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168101
0000132968 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168102
0000132969 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168103
0000132970 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168104
0000132971 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168105
0000132972 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168106
0000132973 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168107
0000132974 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168108
0000132975 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168108
0000132976 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168109
0000132977 - - - Familial, autosomal dominant - - - - - Wang Wenjing 00168110
0000184399 empty follicle syndrome OOMD-1 Empty ovarian follicle (HP:0031067), Female infertility(HP:0008222), Autosomal recessive inheritance(HP:0000007) Familial, autosomal recessive 28y 28y 23y Female infertility (HP:0008222) - Na Li 00165318
0000184404 empty follicle syndrome OOMD-1 Empty ovarian follicle (HP:0031067), Female infertility(HP:0008222), Autosomal recessive inheritance(HP:0000007) Familial, autosomal recessive 23y 23y 20y Female infertility (HP:0008222) - Na Li 00227921
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