Phenotypes for disease #00477 (OCA2 (albinism, oculocutaneous, type II (OCA-2, brown)), OMIM:203200)

10 entries on 1 page. Showing entries 1 - 10.
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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     
0000054351 Mild generalized hypopigmentation (HP:0007513) - - Familial, autosomal recessive 23y - - - - Pieter Klap 00074554
0000054352 Mild generalized hypopigmentation (HP:0007513) - - Familial, autosomal recessive 60y - - - - Pieter Klap 00074555
0000054353 Mild generalized hypopigmentation (HP:0007513) - - Familial, autosomal recessive 21y - - - - Pieter Klap 00074556
0000054364 Mild generalized hypopigmentation (HP:0007513) - - Familial, autosomal recessive 56y - - - - Pieter Klap 00074567
0000079166 - - - Unknown - - - - - Gemeinschaftspraxis für Humangenetik Dresden 00100940
0000275964 anterior segment developmental anomalies including glaucoma; MIM, 137750 or 609887 MIM, 137750 or 609887 - Familial, autosomal dominant - - - - - LOVD 00382122
0000275994 Oculocutaneous albinism and others; - - Familial, autosomal recessive - - - - - LOVD 00382152
0000361833 Retinal dystrophy, central scotoma, visual impairment, nonprogressive visual loss and reduced visual acuity - Oculocutaneous albinism Familial, autosomal recessive - - - - - Mohammed A.M Derar 00477223
0000361834 Nonprogressive visual loss, central scotoma, visual impairment, macular atrophy and reduced visual acuity - oculocutaneous albinism Familial, autosomal recessive - - - - - Mohammed A.M Derar 00477224
0000361835 Visual impairment and foveal hypoplasia - Oculocutaneous albinism Familial, autosomal recessive - - - - - Mohammed A.M Derar 00477225
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