Global Variome shared LOVD
SERHL (serine hydrolase-like)
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Phenotypes for disease #05079 (PBD (peroxisome biogenesis disorder (Zellweger syndrome)))
Legend
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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all entries beginning with 'p.(Arg'
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Date
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Date
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all entries not matching March, 2020
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all entries before the year 2020
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Date
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all entries on or after June 15th, 2020
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all entries in 2019 or 2020, and before March, 2020
Numeric
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all entries lower than 23
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all entries lower than, or equal to, 23
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all entries higher than, or equal to, 23
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Numeric
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all entries with values from 20 to 29, but not equal to 23
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all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc.
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all entries containing 'Asian' but not containing 'Caucasian'
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all entries containing 'Asian' or 'African', but not containing 'Caucasian'
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all entries containing 'South Asian', but not containing 'South East Asian'
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784 entries on 8 pages. Showing entries 1 - 100.
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Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000218063
-
peroxisome biogenesis disorder
-
Unknown
-
-
-
-
-
Julia Lopez
00282884
0000218064
-
peroxisome biogenesis disorder
-
Unknown
-
-
-
-
-
Julia Lopez
00282894
0000218065
see paper; ...
peroxisome biogenesis disorder
-
Familial, autosomal recessive
-
-
-
-
-
Julia Lopez
00283308
0000218066
-
peroxisome biogenesis disorder
type 4
Unknown
-
-
-
-
-
Julia Lopez
00283313
0000218067
see paper; ...
peroxisome biogenesis disorder
-
Familial, autosomal recessive
-
-
-
-
-
Julia Lopez
00283323
0000218068
see paper; ...
peroxisome biogenesis disorder
-
Familial, autosomal recessive
-
-
-
-
-
Julia Lopez
00283335
0000218069
moderate intellectual disability retinitis pigmentosa, hearing loss, ataxia
peroxisome biogenesis disorder
-
Familial, autosomal recessive
-
-
-
-
-
Julia Lopez
00283339
0000218070
-
peroxisome biogenesis disorder
type 4A
Unknown
-
-
-
-
-
Julia Lopez
00283346
0000218073
-
peroxisome biogenesis disorder
type 4A
Unknown
-
-
-
-
-
Julia Lopez
00283364
0000218076
-
peroxisome biogenesis disorder
-
Unknown
-
-
-
-
-
Julia Lopez
00283384
0000218078
-
peroxisome biogenesis disorder
type 4
Unknown
-
-
-
-
-
Julia Lopez
00283387
0000218079
zellweger syndrome
peroxisome biogenesis disorder (NALD/IRD)
type 1B
Unknown
-
-
-
-
-
Julia Lopez
00283625
0000218081
-
peroxisome biogenesis disorder
-
Unknown
-
-
-
-
-
Julia Lopez
00283630
0000218082
-
peroxisome biogenesis disorder
-
Unknown
-
-
-
-
-
Julia Lopez
00283632
0000218085
-
peroxisome biogenesis disorder
-
Unknown
-
-
-
-
-
Julia Lopez
00283637
0000218088
-
peroxisome biogenesis disorder
-
Unknown
-
-
-
-
-
Julia Lopez
00283641
0000218089
-
peroxisome biogenesis disorder
-
Unknown
-
-
-
-
-
Julia Lopez
00283654
0000218090
-
peroxisome biogenesis disorder
-
Unknown
-
-
-
-
-
Julia Lopez
00283656
0000218091
-
peroxisome biogenesis disorder
-
Unknown
-
-
-
-
-
Julia Lopez
00283657
0000218093
-
peroxisome biogenesis disorder
-
Unknown
-
-
-
-
-
Julia Lopez
00283662
0000218094
-
peroxisome biogenesis disorder
-
Unknown
-
-
-
-
-
Julia Lopez
00283665
0000218098
-
peroxisome biogenesis disorder
-
Unknown
-
-
-
-
-
Julia Lopez
00283697
0000218101
-
peroxisome biogenesis disorder
-
Unknown
-
-
-
-
-
Julia Lopez
00283711
0000218103
-
peroxisome biogenesis disorder
-
Unknown
-
-
-
-
-
Julia Lopez
00283725
0000218104
-
peroxisome biogenesis disorder
-
Unknown
-
-
-
-
-
Julia Lopez
00283728
0000218105
-
peroxisome biogenesis disorder
-
Unknown
-
-
-
-
-
Julia Lopez
00283730
0000218896
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283299
0000218898
-
Zellweger syndrome
type C
Unknown
-
-
-
-
-
Julia Lopez
00283301
0000218899
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283302
0000218902
-
Zellweger syndrome
type C
Unknown
-
-
-
-
-
Julia Lopez
00283305
0000218903
-
Zellweger syndrome
type C
Unknown
-
-
-
-
-
Julia Lopez
00283306
0000218904
-
Zellweger syndrome
type C
Unknown
-
-
-
-
-
Julia Lopez
00283307
0000218905
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283309
0000218906
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283310
0000218907
-
Zellweger syndrome
type C
Unknown
-
-
-
-
-
Julia Lopez
00283311
0000218908
-
Zellweger syndrome
type C
Unknown
-
-
-
-
-
Julia Lopez
00283312
0000218911
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283317
0000218915
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283321
0000218917
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283324
0000218922
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283332
0000218926
-
Zellweger syndrome
type C
Unknown
-
-
-
-
-
Julia Lopez
00283338
0000218934
-
Zellweger syndrome
type C
Unknown
-
-
-
-
-
Julia Lopez
00283348
0000218937
-
Zellweger syndrome
type C
Unknown
-
-
-
-
-
Julia Lopez
00283351
0000218938
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283352
0000218939
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283353
0000218940
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283354
0000218941
-
Zellweger syndrome
type C
Unknown
-
-
-
-
-
Julia Lopez
00283355
0000218942
-
Zellweger syndrome
type C
Unknown
-
-
-
-
-
Julia Lopez
00283356
0000218945
-
Zellweger syndrome
type C
Unknown
-
-
-
-
-
Julia Lopez
00283361
0000218946
-
Zellweger syndrome
type C
Unknown
-
-
-
-
-
Julia Lopez
00283363
0000218948
-
Zellweger syndrome
type C
Unknown
-
-
-
-
-
Julia Lopez
00283367
0000218952
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283372
0000218954
-
Zellweger syndrome
type C
Unknown
-
-
-
-
-
Julia Lopez
00283374
0000218955
-
Zellweger syndrome
type C
Unknown
-
-
-
-
-
Julia Lopez
00283376
0000218956
-
Zellweger syndrome
type C
Unknown
-
-
-
-
-
Julia Lopez
00283378
0000218957
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283379
0000218958
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283381
0000218959
-
Zellweger syndrome
type C
Unknown
-
-
-
-
-
Julia Lopez
00283382
0000218961
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283385
0000218962
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283619
0000218963
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283621
0000218964
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283622
0000218969
4m-deceased; large fontanelle, wide sutures; high forehead; broad nasal bridge; hypertelorism; no epicanthus; external ear deformity; sickle foot; poor sucking; gavage feeding; hypotonia; severe psychomotor retardation; seizures; no cataract; no retinitis pigmentosa; optic atrophy; no nystagmus; no hepatomegaly; no liver fibrosis; raised liver enzymes; no renal cysts
Zellweger syndrome
-
Familial, autosomal recessive
00y04m
-
-
-
-
Julia Lopez
00283631
0000218970
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283633
0000218971
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283634
0000218972
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283640
0000218973
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283642
0000218976
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283646
0000218978
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283648
0000218979
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283649
0000218986
large fontanelle, wide sutures; high forehead; broad nasal bridge; hypertelorism; epicanthus; no external ear deformity; no sickle foot; poor sucking; no gavage feeding; hypotonia; severe psychomotor retardation; no seizures; no cataract; no retinitis pigmentosa; optic atrophy; no nystagmus; no hepatomegaly; no liver fibrosis; raised liver enzymes; renal cysts
Zellweger syndrome
-
Familial, autosomal recessive
00y04m
-
-
-
-
Julia Lopez
00283660
0000218987
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283661
0000218989
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283666
0000218990
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283669
0000218992
3m-deceased; large fontanelle, wide sutures; high forehead; broad nasal bridge; hypertelorism; epicanthus; external ear deformity; sickle foot; poor sucking; gavage feeding; hypotonia; severe psychomotor retardation; seizures; hepatomegaly; no liver fibrosis; no raised liver enzymes; calcific stipling
Zellweger syndrome
-
Familial, autosomal recessive
00y03m
-
-
-
-
Julia Lopez
00283671
0000218993
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283673
0000218995
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283676
0000218996
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283678
0000218998
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283682
0000218999
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283683
0000219000
2m-deceased; large fontanelle, wide sutures; high forehead; broad nasal bridge; hypertelorism; epicanthus; external ear deformity; sickle foot; poor sucking; gavage feeding; hypotonia; severe psychomotor retardation; seizures; hepatomegaly; liver fibrosis; raised liver enzymes; renal cysts
Zellweger syndrome
-
Familial, autosomal recessive
00y02m
-
-
-
-
Julia Lopez
00283684
0000219001
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283685
0000219003
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283689
0000219007
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283694
0000219009
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283696
0000219012
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283700
0000219017
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283706
0000219018
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283709
0000219024
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283718
0000219027
1y11m-deceased; high forehead; broad nasal bridge; hypertelorism; no epicanthus; external ear deformity; sickle foot; poor sucking; no gavage feeding; hypotonia; severe psychomotor retardation; no seizures; no cataract; no retinitis pigmentosa; no optic atrophy; no nystagmus; no hepatomegaly; no liver fibrosis; no raised liver enzymes
Zellweger syndrome
-
Familial, autosomal recessive
01y11m
-
-
-
-
Julia Lopez
00283724
0000219029
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283727
0000219030
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283729
0000219033
-
Zellweger syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283733
0000235194
see paper; ...
peroxisome biogenesis disorder
PBD12A
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00309875
0000235195
see paper; ...
Zellweger syndrome
PBD12A
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00309876
0000235196
-
Zellweger syndrome
PBD12A
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00309879
0000235197
see paper; ...
Zellweger syndrome
PBD12A
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00309877
0000235216
see paper; ...,uneventful pregnancy, typical craniofacial dysmorphia including large open fontanelles, high forehead, flat occiput, low/broad nasal bridge, amicrognathia; neurologic abnormalities, including hypotonia; plasma analysis elevated very long chain fatty acids, di- and trihydroxycholestanoic acid, normal phytanic acid level; erythrocyte plasmalogens undetectable; died at 10d
Zellweger syndrome
PBD13A
Familial, autosomal recessive
00y00m10d
-
-
-
-
Johan den Dunnen
00309898
0000235217
see paper; ...,severe cholestasis, hepatomegaly, neuronal migration defect, progressive hypotonia
Zellweger syndrome
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00309899
0000235218
see paper; ...
Zellweger syndrome
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00309901
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