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

5 entries on 1 page. Showing entries 1 - 5.
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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
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