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Phenotypes for disease #07219 (PPK (keratoderma, palmoplantar))
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.
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
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all entries beginning with 'p.(Arg'
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=""
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combination
Text
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Date
2020
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Date
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Date
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Date
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Date
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Date
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Date
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combination
Date
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Numeric
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Numeric
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all entries exactly matching 23 or 24
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Numeric
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all entries not exactly matching 23
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Numeric
<23
all entries lower than 23
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Numeric
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all entries lower than, or equal to, 23
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Numeric
>23
all entries higher than 23
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Numeric
>=23
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combination
Numeric
>=20 <30 !23
all entries with values from 20 to 29, but not equal to 23
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Matches
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all entries containing 'Asian' or 'African', but not containing 'Caucasian'
"South Asian"
all entries containing 'South Asian', but not containing 'South East Asian'
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7 entries on 1 page. Showing entries 1 - 7.
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How to query
Phenotype ID
Diagnosis/Initial
Diagnosis/Definite
Phenotype details
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Owner
Individual ID
0000355928
palmoplantar keratoderma
-
see paper; ..., 2y-palmoplantar keratoderma palms/soles; bilateral hearing loss; hyperkeratosis heels/lateral face both soles/weight-bearing areas, hands lesions mainly located in fingertips; no hair anomalies, no tooth abnormalities
Familial, autosomal recessive
33y
-
-
-
Lucía Miranda-Alcaraz
00471095
0000355929
palmoplantar keratoderma
-
see paper; ..., 2y-palmoplantar keratoderma palms/soles; bilateral hearing loss; hyperkeratosis heels/lateral face both soles/weight-bearing areas, hands lesions mainly located in fingertips; no hair anomalies, no tooth abnormalities
Familial, autosomal recessive
33y
-
-
-
Mónica Mora-Gómez
00466203
0000355930
palmoplantar keratoderma
-
see paper; ..., palmoplantar keratoderma, leukonychia, exuberant curly scalp hair; 2y-progressive development yellowish thickened scaly skin palms/soles ; 10y-19yy-toenail dystrophy; soles diffuse, verrucous hyperkeratosis deep fissuring; thick, bushy hair
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00471096
0000355931
palmoplantar keratoderma
-
see paper; ..., 3y-alterations skin both hands/feet, hair, dystrophic nails; thin/curly/sparse hair, long upper eyelid eyelashes, poor dental enamel
Familial, autosomal recessive
60y
-
-
-
Johan den Dunnen
00471097
0000355932
palmoplantar keratoderma
-
see paper; ..., 1d no erythroderma, no neonatal teeth; 2y-keratoderma ingertips, severe diffuse keratoderma with coarse white–yellow scales, painful fissures soles; fingernails mild leuconychia, dystrophic cuticles.; toenails white/brown discoloration, dystrophic with transverse ridges; long curly scalp hair, normal hair growth
Familial, autosomal recessive
26y
-
-
-
Johan den Dunnen
00471098
0000355933
palmoplantar keratoderma
-
see paper; ..., 3y-mild diffuse plantar keratoderma distal heels/distal hallux, painful fissures; nails dysplastic, thin/transverse ridges, white/opaque fingernails, dystrophic toenails; normal teeth, normal hair, normal sweating; 8y-mild scaly hyperkeratosis fingertips, palmar hyperlinearity, dystrophic cuticles with erythematous surrounding skin, mild keratotic plaques/keratosis pilaris skin extensor sides knees/elbows
Familial, autosomal recessive
08y
-
-
-
Johan den Dunnen
00471099
0000355934
footpad hyperkeratosis
-
see paper; ...
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00471100
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