Legend
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Diagnosis/Initial: initial diagnosis, before molecular testing
Diagnosis/Definite: phenotype individual after molecular testing (OMIM abbreviation)
Phenotype details: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
Inheritance: Indicates the inheritance of the phenotype in the family; unknown, familial (autosomal/X-linked, dominant/ recessive), paternal (Y-linked), maternal (mitochondrial), isolated (sporadic) or complex
All options:
- Unknown
- Familial
- Familial, autosomal dominant
- Familial, autosomal recessive
- Familial, X-linked
- Familial, X-linked dominant
- Familial, X-linked dominant, male sparing
- Familial, X-linked recessive
- Paternal, Y-linked
- Maternal, mitochondrial
- Isolated (sporadic)
- Di-genic
- Complex
- - = Not applicable
Age/Examination: age at which the individual was examined.
- 35y = 35 years
- 04y08m = 4 years and 8 months
- 00y00m01d12h = 1 day and 12 hours
- 18y? = around 18 years
- 30y-40y = between 30 and 40 years
- >54y = older than 54
- ? = unknown
Age/Diagnosis: age diagnosis was confirmed
- 35y = 35 years
- 04y08m = 4 years and 8 months
- 00y00m01d12h = 1 day and 12 hours
- 18y? = around 18 years
- 30y-40y = between 30 and 40 years
- >54y = older than 54
- ? = unknown
Age/Onset: Age first symptoms disease appeared in individual:
- 35y = 35 years
- 04y08m = 4 years and 8 months
- 00y00m01d12h = 1 day and 12 hours
- 18y? = around 18 years
- 30y-40y = between 30 and 40 years
- >54y = older than 54
- ? = unknown
Phenotype/Onset: individual's phenotype at Age/Onset described using HPO

 Phenotype ID
|

 Diagnosis/Initial
|

 Diagnosis/Definite
|

 Phenotype details
|

 Inheritance
|

 Age/Examination
|

 Age/Diagnosis
|

 Age/Onset
|

 Phenotype/Onset
|

 Owner
|

 Individual ID
|
0000157642 |
oculocutaneous albinism |
OCA-1A |
Oculocutaneous albinism |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00209036 |
0000242973 |
Albinism |
Albinism |
Exotropia, Nystagmus, Anomalous head posture, grade 1 iris transillumination defects, VEP misrouting, |
Familial, autosomal recessive |
09y |
09y |
- |
- |
Mervyn Thomas |
00324431 |
0000242974 |
?Albinism carrier |
- |
Reduced visual acuity (0.15 and 0.225 logMAR). VEP misrouting |
Familial, autosomal recessive |
09y |
09y |
- |
- |
Mervyn Thomas |
00324432 |
0000242976 |
- |
- |
Reduced VA (0.85 logMAR), Nystagmus, anomalous head posture, grade 4 foveal hypoplasia, grade 4 transillumination defects of iris |
Familial, autosomal recessive |
05y |
05y |
- |
<6m |
Mervyn Thomas |
00324434 |
0000242999 |
albinism |
albinism |
nystagmus, anomalous head posture, grade 1 foveal hypoplasia, misrouting on VEP |
Familial, autosomal recessive |
05y |
05y |
- |
- |
Mervyn Thomas |
00324429 |
0000243558 |
oculocutaneous albinism |
- |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325071 |
0000243559 |
oculocutaneous albinism |
- |
see paper; ..., residual pigmentation hairs and iris; iris blue; hair golden brown; no nystagmus; no strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325072 |
0000243573 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325087 |
0000243574 |
oculocutaneous albinism |
OCA1 |
iris brownish yellow; hair white; nystagmus; no strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325088 |
0000243575 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325089 |
0000243576 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325090 |
0000243577 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325091 |
0000243578 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325092 |
0000243579 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325093 |
0000243580 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325094 |
0000243581 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325095 |
0000243582 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325096 |
0000243583 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325097 |
0000243584 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325098 |
0000243585 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325099 |
0000243586 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325100 |
0000243587 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325101 |
0000243588 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325102 |
0000243589 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325103 |
0000243590 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; no nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325104 |
0000243591 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; no nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325105 |
0000243592 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325106 |
0000243593 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325107 |
0000243594 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325108 |
0000243595 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325109 |
0000243596 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325110 |
0000243597 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325111 |
0000243598 |
oculocutaneous albinism |
OCA1 |
iris brownish yellow; hair white; nystagmus; no strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325112 |
0000243599 |
oculocutaneous albinism |
OCA1 |
iris brownish yellow; hair white; nystagmus; no strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325113 |
0000243600 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325114 |
0000243601 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325115 |
0000243602 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325116 |
0000243603 |
oculocutaneous albinism |
OCA1 |
iris translucent; hair white; nystagmus; strabismus |
Familial, autosomal recessive |
- |
- |
- |
- |
Mainak Sengupta |
00325117 |
0000253858 |
- |
- |
Brown OCA, Rufous OCA |
Unknown |
- |
- |
- |
- |
William (Bill) Oetting |
00204373 |
0000253859 |
- |
- |
Brown OCA, Rufous OCA |
Unknown |
- |
- |
- |
- |
William (Bill) Oetting |
00204364 |
0000253860 |
- |
- |
Brown OCA, Rufous OCA |
Unknown |
- |
- |
- |
- |
William (Bill) Oetting |
00204360 |
0000273168 |
albinism, oculocutaneous |
- |
HP:0030515 HP:0001129 HP:0000639, HP:0000007, HP:0001022, HP:0007750, HP:0007894 |
Familial, autosomal recessive |
- |
- |
- |
- |
Jinu Han |
00378022 |
0000273170 |
albinism, oculocutaneous |
- |
HP:0030515 HP:0001129 HP:0000639, HP:0000007, HP:0001022, HP:0007750, HP:0007894 |
Familial, autosomal recessive |
- |
- |
- |
- |
Jinu Han |
00378025 |
0000273483 |
albinism, oculocutaneous |
- |
HP:0030515 HP:0001129 HP:0000639, HP:0000007, HP:0001022, HP:0007750, HP:0002286 |
Familial, autosomal recessive |
- |
- |
- |
- |
Jinu Han |
00379639 |
0000273499 |
albinism, oculocutaneous |
- |
HP:0032037 HP:0000662 HP:0000613, HP:0000639, HP:0000006, HP:0001022, HP:0007750 |
Familial, autosomal dominant |
- |
- |
- |
- |
Jinu Han |
00379655 |
0000273636 |
albinism, oculocutaneous |
- |
HP:0000613, HP:0007730, HP:0007513 |
Familial, autosomal recessive |
- |
- |
- |
- |
Jinu Han |
00379781 |
0000278906 |
OCA |
OCA |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
Barbara Vona |
00385125 |
0000292438 |
Albinism |
Foveal Hypoplasia 2 |
Hypoplasia of the fovea (HP:0007750), reduced visual acuity (HP:0007663), nystagmus (HP:0000639), optic nerve misrouting (HP:0025551), iris transillumination defect (HP:0012805) and strabismus (HP:0000486) |
Familial, autosomal recessive |
- |
36y |
- |
rs1161159416 |
Mohammed A.M Derar |
00399319 |
0000317353 |
oculocutaneous albinism |
OCA2 |
- |
Familial, autosomal recessive |
03y |
- |
- |
- |
Johan den Dunnen |
00426125 |
0000326761 |
- |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
Sudha Kohli, Renu Saxena, Ratna Puri, I.C. Verma |
00436619 |
0000350869 |
- |
606952 |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
Gemeinschaftspraxis für Humangenetik Dresden |
00465316 |