Global Variome shared LOVD
HNF4A (hepatocyte nuclear factor 4, alpha)
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Curator:
Kevin Colclough
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Phenotypes for disease #05595 (CS (Cockayne syndrome (CS)))
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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Date
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9 entries on 1 page. Showing entries 1 - 9.
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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
0000173469
Cockayne syndrome
CSA
-
-
-
-
-
-
SIB - Livia Famiglietti
00230985
0000173470
Cockayne syndrome
CSA
-
-
-
-
-
-
SIB - Livia Famiglietti
00230986
0000173471
Cockayne syndrome
CSA
-
-
-
-
-
-
SIB - Livia Famiglietti
00230987
0000173472
Cockayne syndrome
CSA
-
-
-
-
-
-
SIB - Livia Famiglietti
00230988
0000173473
Cockayne syndrome
CSA
-
-
-
-
-
-
SIB - Livia Famiglietti
00230989
0000173474
Cockayne syndrome
CSA
-
-
-
-
-
-
SIB - Livia Famiglietti
00230990
0000231958
Cockayne syndrome type II
-
uneventful antenatal period;4-6m microcephaly, micrognathia, contractures knees and elbows, hypertonic, dislocated radial head, deep-set eyes, skeletal abnormalities, camptodactyly, adducted thumbs, stiff limbs, steeply sloping acetabulae, wrist contracture, slender long bones with mildly flared metaphyses, moderate kyphoscoliosis; brisk reflexes, no feeding problems; MRI brain at birth possible polymicrogyria; NMR 4m-large bilateral subdurals (>2 cm in depth), no major visible malformations; ECG 9m-abnormal; 16m-nystagmus, no other ophthalmic abnormalities, corneas completely clear, no cataracts; 2.5y-deceased
Familial, autosomal recessive
02y06m
-
-
-
Johan den Dunnen
00306117
0000231962
Cockayne syndrome
-
prenatal microcephaly; born 41w, weight 2.9 kg, OFC 9th percentile first few months, OFC 1y-<2nd percentile; first year developed normally; 5y-multiple unusual plantar warts hands and forearms, unusual freckling hands and back of neck, tended to burn easily and quickly, no bad blisterering when exposed to sunlight; 7y-deep-set eyes, progressive scoliosis, multiple contractures feet, required lengthening Achilles tendon because of muscle cramps in hamstrings and calves; skin deeply pigmented, rashes, flat freckles; moderate bilateral hearing impairment, especially higher tones (<3y-normal hearing), short stature (height 110.4 cm [<2nd percentile], weight of 16.3 kg [<3rd percentile]), microcephaly (OFC 45.5 cm [<2nd percentile]), circulatory problems, bilateral astigmatism, no cataracts, attention deficit hyperactivity disorder, learning disability; MRI brain 3y-some delayed myelination, 7y-basal ganglia T1 shortening; severe migraines and headaches, ambulation lessened over time, gastrostomy-jejunostomy tube for feeding
Familial, autosomal recessive
16y
-
-
-
Johan den Dunnen
00306119
0000231965
Cockayne syndrome
-
see paper; ..., 12y-deceased
Familial, autosomal recessive
12y
-
-
-
Johan den Dunnen
00306122
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