Global Variome shared LOVD
UBA1 (ubiquitin-like modifier activating enzyme 1)
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Phenotypes for disease #00472 (OAS (oculo-auricular syndrome (OAS)), OMIM:612109)
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Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
Diagnosis/Initial
: initial diagnosis, before molecular testing
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
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
Protein
: result from protein staining
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Date
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18 entries on 1 page. Showing entries 1 - 18.
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How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000017010
microphthalmia, microcornea, sclerocornea, posterior embryotoxon, congenital cataract, iris coloboma, uveoretinal coloboma, early-onset retinal dystrophy, dysplastic optic discs, low-set ears, malformation of the external ear cartilage
-
-
Familial, autosomal recessive
00y04m
-
-
-
-
Rachel Gillespie
00018566
0000299002
Microtia (HPO:0008551), atresia of the external auditory canal (HPO:0000403), conductive hearing impairment (HPO:0000405), ossicular chain abnormality (HPO:004452), hemifacial hypoplasia (HPO:0011332)
Microtia
OAVS
Complex
03y
-
-
-
TCOF1
Miriam Erandi Reyna-Fabián
00406527
0000299004
Microtia (HPO:0008551), stenosis of the external auditory canal (HPO:0000402), conductive hearing impairment (HPO:0000405), ossicular chain abnormality (HPO:004452), facial paralysis (HP:0007209)
Microtia
OAVS
Complex
02y05m
-
-
-
TCOF1
Miriam Erandi Reyna-Fabián
00406530
0000300580
Microtia (HPO:0008551), hemifacial hypoplasia (HPO:0011332), facial paralysis (HP:0007209), Vertebral clefting (HP:0008428)
Microtia
OAVS
Unknown
03y05m
-
-
-
TCOF1
Miriam Erandi Reyna-Fabián
00408464
0000300581
Microtia (HPO:0008551), atresia of the external auditory canal (HPO:0000403), ossicular chain abnormality (HPO:004452), conductive hearing impairment (HPO:0000405)
Microtia
OAVS
Unknown
02y07m
-
-
-
TCOF1
Miriam Erandi Reyna-Fabián
00408466
0000300670
Microtia (HPO:0008551), atresia of the external auditory canal (HPO:0000413), conductive hearing impairment (HPO:0000405), ossicular chain abnormality (HPO:004452)
microtia
OAVS
Unknown
02y05m
-
-
-
TCOF1
Miriam Erandi Reyna-Fabián
00408552
0000300938
Microtia (HPO:0008551), atresia of the external auditory canal (HPO:0000413), conductive hearing impairment (HPO:0000405), ossicular chain abnormality (HPO:004452), Vertebral clefting (HP:0008428)
Microtia
OAVS
Familial
06y
-
-
-
SALL1
Miriam Erandi Reyna-Fabián
00408819
0000300939
Microtia (HPO:0008551), atresia of the external auditory canal (HPO:0000413), ossicular chain abnormality (HPO:004452), conductive hearing impairment (HPO:0000405), supernumerary ribs (HPO:0005815)
Microtia
OAVS
Unknown
06y11m
-
-
-
SALL1
Miriam Erandi Reyna-Fabián
00408820
0000300940
Microtia (HPO:0008551), atresia of the external auditory canal (HPO:0000413), conductive hearing impairment (HPO:0000405), ossicular chain abnormality (HPO:004452), Vertebral clefting (HP:0008428)
Microtia
OAVS
Familial
10y
-
-
-
SALL1
Miriam Erandi Reyna-Fabián
00408821
0000300941
Microtia (HPO:0008551), atresia of the external auditory canal (HPO:0000413),conductive hearing impairment (HPO:0000405), ossicular chain abnormality (HPO:004452), hemifacial hypoplasia (HPO:0011332)
Microtia
OAVS
Unknown
02y
-
-
-
SALL1
Miriam Erandi Reyna-Fabián
00408822
0000300942
Microtia (HPO:0008551), atresia of the external auditory canal (HPO:0000413), conductive hearing impairment (HPO:0000405), ossicular chain abnormality (HPO:004452).
Microtia
OAVS
Unknown
-
06y11m
-
-
SALL1
Miriam Erandi Reyna-Fabián
00408823
0000300943
Microtia (HPO:0008551), atresia of the external auditory canal (HPO:0000413), conductive hearing impairment (HPO:0000405), ossicular chain abnormality (HPO:004452).
Microtia
OAVS
Unknown
-
06y11m
-
-
SALL1
Miriam Erandi Reyna-Fabián
00408824
0000300944
Microtia (HPO:0008551), atresia of the external auditory canal (HPO:0000413), conductive hearing impairment (HPO:0000405), ossicular chain abnormality (HPO:004452), hemifacial hypoplasia (HPO:0011332).
Microtia
OAVS
Unknown
02y09m
-
-
-
SALL1
Miriam Erandi Reyna-Fabián
00408825
0000300946
Microtia (HPO:0008551), atresia of the external auditory canal (HPO:0000413), conductive hearing impairment (HPO:0000405), ossicular chain abnormality (HPO:004452), hemifacial hypoplasia (HPO:0011332).
Microtia
OAVS
Unknown
02y03m
-
-
-
TBX1
Miriam Erandi Reyna-Fabián
00408828
0000300950
Microtia (HPO:0008551), atresia of the external auditory canal (HPO:0000413), sensorineural hearing impairment (HPO:0000407), ossicular chain abnormality (HPO:004452).
Microtia
OAVS
Unknown
07y08m
-
-
-
TBX1
Miriam Erandi Reyna-Fabián
00408832
0000300951
Microtia (HPO:0008551), atresia of the external auditory canal (HPO:0000413), conductive hearing impairment (HPO:0000405), ossicular chain abnormality (HPO:004452), hemifacial hypoplasia (HPO:0011332).
Microtia
OAVS
Unknown
06y
-
-
-
EYA1
Miriam Erandi Reyna-Fabián
00408827
0000301106
Microtia (HPO:0008551), atresia of the external auditory canal (HPO:0000413), conductive hearing impairment (HPO:0000405), ossicular chain abnormality (HPO:004452).
-
-
Unknown
16y
-
-
-
TCOF1
Miriam Erandi Reyna-Fabián
00408988
0000301107
Microtia (HPO:0008551), atresia of the external auditory canal (HPO:0000413), conductive hearing impairment (HPO:0000405), sensorineural hearing impairment (HPO:0000407), renal hypoplasia (HPO:0008678)
Microtia
OAVS
Unknown
05y08m
-
-
-
SALL1
Miriam Erandi Reyna-Fabián
00408989
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