Phenotypes for disease #00474 (OCA1B (albinism, oculocutaneous, type IB (OCA-1B)), OMIM:606952)

43 entries on 1 page. Showing entries 1 - 43.
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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     
0000054355 Mild generalized hypopigmentation (HP:0007513) - - Familial, autosomal recessive 29y - - - - Pieter Klap 00074557
0000054356 Mild generalized hypopigmentation (HP:0007513) - - Familial, autosomal recessive 18y - - - - Pieter Klap 00074559
0000054362 Mild generalized hypopigmentation (HP:0007513) - - Familial, autosomal recessive 31y - - - - Pieter Klap 00074565
0000069344 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089972
0000069345 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089973
0000069346 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089974
0000069347 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089975
0000069348 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089976
0000069349 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089977
0000069350 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089978
0000069351 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089979
0000069352 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089980
0000069353 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089981
0000069354 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089982
0000069355 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089983
0000069356 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089984
0000069357 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089985
0000069358 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089986
0000069359 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089987
0000069360 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089988
0000069361 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089989
0000069362 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089990
0000069363 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089991
0000069364 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089992
0000069365 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089993
0000069366 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089994
0000069367 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089995
0000069368 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089996
0000069369 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089997
0000069370 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089998
0000069371 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00089999
0000069372 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00090000
0000069373 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00090001
0000069374 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00090002
0000069375 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00090003
0000069376 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00090004
0000069377 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00090005
0000069378 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00090006
0000069379 oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00090007
0000069380 ?oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00090008
0000069381 ?oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00090009
0000069382 ?oculocutaneous albinism type IB - - Familial, autosomal recessive - - - - - William (Bill) Oetting 00090010
0000069480 tyrosinase positive OCA, pale-yellow scalp hair, white eyebrows, nystagmus, photophobia, strabismus, decreased visual acuity, one pigmented compound nevus neck, several flesh-colored halo nevi, port wine stain lower lumbar region - - Familial, autosomal recessive 08y - - - - Johan den Dunnen 00090099
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