Phenotypes for disease #02923 (ASGD2 (dysgenesis, anterior segment, type 2 (ASGD-2, aphakia, congenital primary)), OMIM:610256)

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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     
0000051145 congenital primary aphakia, microphthalmia, sclerocornea - - Familial, autosomal recessive - - - - - Deepti Anand 00064999
0000051146 congenital primary aphasia, microphthalmia, sclerocornea - - Familial, autosomal recessive - - - - - Deepti Anand 00064997
0000051149 congenital primary aphasia as primary phenotype, aplasia of the anterior segment of the eye, iris absent, microphthalmia, retinal dysplasia - - Familial, autosomal recessive - - - - - Deepti Anand 00064992
0000051150 congenital primary aphasia, glaucoma, microcornea, Peters anomaly, sclerocornea - - Familial, autosomal recessive - - - - - Deepti Anand 00064993
0000051151 congenital primary aphakia, microphthalmia, corneal opacity, iris absent - - Familial, autosomal recessive - - - - - Deepti Anand 00064994
0000051152 congenital cataract and primary aphasia, coloboma, microphthalmia, sclerocornea, Peters anomaly - - Familial, autosomal dominant - - - - - Deepti Anand 00064995
0000051154 congenital primary aphakia - - Familial, autosomal recessive - - - - - Deepti Anand 00065000
0000051163 congenital primary aphakia, anophthalmia, corneal opacity - - Familial, autosomal recessive - - - - - Deepti Anand 00065011
0000051165 see paper; ..., - - Familial, autosomal recessive - - - - - Johan den Dunnen 00065013
0000353682 see paper; ..., anterior segment dysgenesis, Peters anomaly anterior segment dysgenesis ASGD2 Familial, autosomal dominant - - - - - Johan den Dunnen 00468529
0000353717 see paper; ..., primary aphakia, bilateral congenital corneal opacity, glaucoma; iridocorneal adhesion ocular anterior segment disease ASGD2 Familial, autosomal recessive - - - - - Johan den Dunnen 00468563
0000353718 see paper; ..., primary aphakia, bilateral congenital corneal opacity, glaucoma ocular anterior segment disease ASGD2 Familial, autosomal recessive - - - - - Johan den Dunnen 00468564
0000353719 see paper; ..., primary aphakia, bilateral congenital corneal opacity, glaucoma ocular anterior segment disease ASGD2 Familial, autosomal recessive - - - - - Johan den Dunnen 00468565
0000354851 see paper; ..., Peters anomaly, bilateral corneal opacities, developmental glaucoma, iris–retina coloboma (3/4), anterior segment dysgenesis, iridolenticular adhesions, nystagmus (3/4); no skeletal abnormalities, no physical disabilities, no cardiovascular diseases, no intellectual disability Peters anomaly ASGD2 Familial, autosomal recessive - - - - - Johan den Dunnen 00469699
0000354854 see paper; ..., severe bilateral ocular dysgenesis, unilateral staphylomatous malformation, complex microphthalmos, bilateral aphakia, unilateral anterior staphyloma anterior segment dysgenesis ASGD2 Familial, autosomal recessive - - - - - Johan den Dunnen 00469702
0000354855 see paper; ..., bilateral microphthalmia, corneal opacity, anterior segment dysgenesis anterior segment dysgenesis ASGD2 Familial, autosomal recessive - - - - - Johan den Dunnen 00469703
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