Global Variome shared LOVD
LRRK1 (leucine-rich repeat kinase 1)
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Phenotypes for disease #00194 (AFD1 (dysostosis, acrofacial, type 1, (AFD-1, Nager type)), OMIM:154400)
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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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26 entries on 1 page. Showing entries 1 - 26.
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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
0000058321
Nager syndrome; Downslanted palpebral fissures; absent lower eyelashes (sparse); midface retrusion; micrognathia; cleft soft palate; abnormal ears; hearing loss; abnormal thumbs (stiff bilateral); radioulnar synostosis (bilateral)
-
-
Isolated (sporadic)
5y
-
-
-
-
Johan den Dunnen
00078550
0000058322
Nager syndrome; Downslanted palpebral fissures; micrognathia; radioulnar synostosis; valgus laxity of knees and ankles
-
-
Isolated (sporadic)
38y
-
-
-
-
Johan den Dunnen
00078551
0000058323
Nager syndrome; Micrognathia; cleft palate; tracheotomy; hearing loss; radioulnar synostosis; subglottic stenosis
-
-
Familial, autosomal dominant
1y
-
-
-
-
Johan den Dunnen
00078552
0000058324
Nager syndrome; Downslanted palpebral fissures; absent lower eyelashes; midface retrusion; micrognathia; ankylosis of temporomandibular joint; high arched, cleft soft palate; tracheotomy; abnormal ears; hearing loss; absent right thumb and small and stiff left thumb; radioulnar synostosis; delayed development; limited range of movement in elbows and shoulders, camptodactyly, left clubfoot, renal abnormalities, ventriculoseptal defect and dacryostenosis
-
-
Isolated (sporadic)
13y
-
-
-
-
Johan den Dunnen
00078553
0000058325
Nager syndrome
-
-
Isolated (sporadic)
15y
-
-
-
-
Johan den Dunnen
00078554
0000058326
Nager syndrome; Absent lower eyelashes (minimal); midface retrusion; micrognathia; abnormal soft palate; abnormal ears; hearing loss; radial ray abnormality; absent thumbs (bilateral); hair extension on cheek, strabismus, mitral valve prolapse, and limited range of movement in elbows
-
-
Isolated (sporadic)
1y
-
-
-
-
Johan den Dunnen
00078555
0000058327
Nager syndrome; Downslanted palpebral fissures; midface retrusion; micrognathia; abnormal palate; abnormal ears; hearing loss; radial ray abnormality; abnormal thumbs; radioulnar synostosis; intellectual disability
-
-
Isolated (sporadic)
2y
-
-
-
-
Johan den Dunnen
00078556
0000058328
Nager syndrome; Downslanted palpebral fissures; absent lower eyelashes; midface retrusion; micrognathia; tracheotomy; abnormal ears; hearing loss; abnormal thumbs
-
-
Familial, autosomal dominant
17y
-
-
-
-
Johan den Dunnen
00078557
0000058329
Nager syndrome; Downslanted palpebral fissures; micrognathia
-
-
Isolated (sporadic)
56y
-
-
-
-
Johan den Dunnen
00078558
0000058330
Nager syndrome; Downslanted palpebral fissures; absent lower eyelashes (decreased); midface retrusion; micrognathia; abnormal soft palate; abnormal ears; hearing loss; radial ray abnormality; abnormal thumbs (proximally placed and stiff); radioulnar synostosis (right)
-
-
Isolated (sporadic)
2y
-
-
-
-
Johan den Dunnen
00078559
0000058331
Nager syndrome; Downslanted palpebral fissures; midface retrusion; micrognathia; high arched palate; tracheotomy; abnormal ears; radial ray abnormality; abnormal thumbs; short stature and bilateral syndactyly of the 4th and 5th toes
-
-
Isolated (sporadic)
4y
-
-
-
-
Johan den Dunnen
00078560
0000058332
Nager syndrome; Micrognathia; ankylosis of temporomandibular joint; cleft palate; tracheotomy; hearing loss; radial ray abnormality; abnormal thumbs (absent bilateral); radioulnar synostosis
-
-
Isolated (sporadic)
12y
-
-
-
-
Johan den Dunnen
00078561
0000058333
Nager syndrome; Downslanted palpebral fissures; absent lower eyelashes; micrognathia; hearing loss; radial ray abnormality; absent left thumb and fused right distal interphalangeal joint; radioulnar synostosis; limited range of motion in all extremities at birth, arachnodactyly, and small 5th fingers
-
-
Isolated (sporadic)
4y
-
-
-
-
Johan den Dunnen
00078562
0000058334
Nager syndrome; Downslanted palpebral fissures; midface retrusion; micrognathia; tracheotomy; abnormal ears; radial ray abnormality; abnormal thumbs; radioulnar synostosis; ventriculoseptal defect and diaphragmatic hernia
-
-
Isolated (sporadic)
4y
-
-
-
-
Johan den Dunnen
00078563
0000058335
Nager syndrome; Downslanted palpebral fissures; absent lower eyelashes; midface retrusion; micrognathia; tracheotomy; abnormal ears; hearing loss; small right thumb and slender left thumb; radioulnar synostosis (unilateral); abnormal teeth, partial absence of left fingers 3-5, slencer haluces, and hallux valgus
-
-
Isolated (sporadic)
24y
-
-
-
-
Johan den Dunnen
00078564
0000058336
Nager syndrome; Downslanted palpebral fissures; absent lower eyelashes (sparse); midface retrusion; micrognathia; abnormal ears; hearing loss; small abnormal thumbs
-
-
Isolated (sporadic)
28y
-
-
-
-
Johan den Dunnen
00078565
0000058337
Nager syndrome; Downslanted palpebral fissures; midface retrusion; micrognathia; cleft palate; tracheotomy; abnormal ears; radial ray abnormality (absent bilateral); abnormal thumbs (absent bilateral); delayed development; fused 1st and 2nd right metacarpals and bilateral foot deformities
-
-
Isolated (sporadic)
2y
-
-
-
-
Johan den Dunnen
00078566
0000058338
Nager syndrome; Downslanted palpebral fissures; micrognathia; abnormal soft palate; abnormal ears; hearing loss; absent right thumb and small left thumb
-
-
Familial, autosomal dominant
1y
-
-
-
-
Johan den Dunnen
00078567
0000058339
Nager syndrome; Downslanted palpebral fissures; micrognathia; abnormal soft palate; abnormal ears; hearing loss; small abnormal thumbs; radioulnar synostosis (bilateral)
-
-
Isolated (sporadic)
28y
-
-
-
-
Johan den Dunnen
00078568
0000058340
Nager syndrome; Downslanted palpebral fissures; midface retrusion; micrognathia; abnormal ears (mild); hearing loss; abnormal thumbs (hypoplasia); radioulnar synostosis (bilateral); speech delay; asymmetric face, velopharyngeal insufficiency; and cervical ribs
-
-
Isolated (sporadic)
23y
-
-
-
-
Johan den Dunnen
00078569
0000058341
Nager syndrome; Downslanted palpebral fissures; midface retrusion; cleft palate; abnormal ears (cupped); hearing loss; abnormal thumbs (small)
-
-
Isolated (sporadic)
49y
-
-
-
-
Johan den Dunnen
00078570
0000058342
Nager syndrome; Downslanted palpebral fissures; absent lower eyelashes (sparse); midface retrusion; micrognathia; tracheotomy; abnormal ears (cupped, narrow canals); hearing loss; absent right thumb and small left thumb; radioulnar synostosis (right > left); delayed speech and fine motor; short stature (3-5%), dacryostenosis, and small first toes and first metatarsals
-
-
Familial, autosomal dominant
20y
-
-
-
-
Johan den Dunnen
00078571
0000058343
Nager syndrome; Downslanted palpebral fissures; absent lower eyelashes; midface retrusion; micrognathia; abnormal palate; abnormal ears (cupped, narrow canals); hearing loss; small right thumb compared to left; radioulnar synostosis (left); delayed development; dacryostenosis, short first metatarsals, and sandal gap
-
-
Familial, autosomal dominant
17y
-
-
-
-
Johan den Dunnen
00078572
0000058344
Nager syndrome; Absent lower eyelashes; micrognathia; cleft palate; hearing loss; radial ray abnormality; abnormal thumbs
-
-
Isolated (sporadic)
5y
-
-
-
-
Johan den Dunnen
00078573
0000058345
Nager syndrome; Downslanted palpebral fissures; midface retrusion; micrognathia; abnormal palate; abnormal ears; hearing loss; radial ray abnormality (short); abnormal thumbs (stiff bilateral)
-
-
Familial, autosomal dominant
7y
-
-
-
-
Johan den Dunnen
00078574
0000058346
Nager syndrome
-
-
Familial, autosomal dominant
-
-
-
-
-
Eva Trevisson
00078575
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