Global Variome shared LOVD
TGIF1 (TGFB-induced factor homeobox 1)
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Phenotypes for disease #00260 (CFND;CFNS (dysplasia, craniofrontonasal (CFND, craniofrontonasal syndrome (CFNS))), OMIM:304110)
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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Date
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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
0000001950
Sprengel deformity; coronal craniosynostosis (left/right); no cleft lip; no cleft palate; no duplex thumb/hallux; no agenesis corpus callosum
-
-
Familial, X-linked dominant
-
-
-
-
-
Jacqueline Goos
00003095
0000001953
-
-
-
Familial, X-linked dominant
-
-
-
-
-
Jacqueline Goos
00003096
0000001954
-
-
-
Familial, X-linked dominant
-
-
-
-
-
Jacqueline Goos
00003097
0000001955
Sprengel deformity; coronal craniosynostosis (left/right); no cleft lip; no cleft palate; no duplex thumb/hallux; no agenesis corpus callosum
-
-
Familial, X-linked dominant
-
-
-
-
-
Jacqueline Goos
00003109
0000001956
-
-
-
Familial, X-linked dominant
-
-
-
-
-
Jacqueline Goos
00003110
0000001957
-
-
-
Familial, X-linked dominant
-
-
-
-
-
Jacqueline Goos
00003098
0000001958
-
-
-
Familial, X-linked dominant
-
-
-
-
-
Jacqueline Goos
00003099
0000001959
coronal craniosynostosis (left/right); no cleft lip; no cleft palate; no duplex thumb/hallux; no agenesis corpus callosum
-
-
Familial, X-linked dominant
-
-
-
-
-
Jacqueline Goos
00003101
0000001960
-
-
-
Familial, X-linked dominant
-
-
-
-
-
Jacqueline Goos
00003100
0000001974
-
-
-
Familial, X-linked dominant
-
-
-
-
-
Jacqueline Goos
00003102
0000001979
no coronal craniosynostosis (left/right); no cleft lip; cleft palate (uvula); duplex thumb right; agenesis corpus callosum; developmental delay
-
-
Familial, X-linked dominant
-
-
-
-
-
Jacqueline Goos
00003103
0000001981
-
-
-
Familial, X-linked dominant
-
-
-
-
-
Jacqueline Goos
00003104
0000001982
coronal craniosynostosis (left/right); no cleft lip; no cleft palate; no duplex thumb/hallux; no agenesis corpus callosum; developmental delay
-
-
Familial, X-linked dominant
-
-
-
-
-
Jacqueline Goos
00003106
0000001984
-
-
-
Familial, X-linked dominant
-
-
-
-
-
Jacqueline Goos
00003107
0000001986
no coronal craniosynostosis (left/right); no cleft lip; no cleft palate; no duplex thumb/hallux
-
-
Familial, X-linked dominant
-
-
-
-
-
Jacqueline Goos
00003108
0000001987
-
-
-
Familial, X-linked dominant
-
-
-
-
-
Jacqueline Goos
00003094
0000001989
-
-
-
Familial, X-linked dominant
-
-
-
-
-
Jacqueline Goos
00003105
0000001990
coronal craniosynostosis left; no cleft lip; no cleft palate; duplex hallux right; no agenesis corpus callosum; developmental delay
-
-
Familial, X-linked dominant
-
-
-
-
-
Jacqueline Goos
00003115
0000001992
-
-
-
Familial, X-linked dominant
-
-
-
-
-
Jacqueline Goos
00003111
0000001993
-
-
-
Familial, X-linked dominant
-
-
-
-
-
Jacqueline Goos
00003116
0000001994
-
-
-
Familial, X-linked dominant
-
-
-
-
-
Jacqueline Goos
00003112
0000001995
-
-
-
Familial, X-linked dominant
-
-
-
-
-
Jacqueline Goos
00003113
0000002036
no coronal craniosynostosis (left/right); no cleft lip; no cleft palate; no duplex thumb/hallux; no agenesis corpus callosum
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00003196
0000002037
coronal craniosynostosis (left/right); no cleft lip; no cleft palate; no duplex thumb/hallux; no agenesis corpus callosum; hypertrophic cardiomyopathy
-
-
Familial
-
-
-
-
-
Johan den Dunnen
00003197
0000002038
coronal craniosynostosis right; no cleft lip; no cleft palate; no duplex thumb/hallux; agenesis corpus callosum; duplex kidney; Bartholin cyst
-
-
Familial
-
-
-
-
-
Johan den Dunnen
00003198
0000002039
no coronal craniosynostosis (left/right); no cleft lip; no cleft palate; duplex hallux left; partial agenesis corpus callosum
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00003199
0000002040
coronal craniosynostosis left; no cleft lip; no cleft palate; no duplex thumb/hallux; no agenesis corpus callosum; diaphragmatic hernia (son)
-
-
Familial
-
-
-
-
-
Johan den Dunnen
00003200
0000002041
coronal craniosynostosis right; no cleft lip; no cleft palate; no duplex thumb/hallux; no agenesis corpus callosum
-
-
Familial
-
-
-
-
-
Johan den Dunnen
00003201
0000002042
no coronal craniosynostosis (left/right); no cleft lip; no cleft palate; no duplex thumb/hallux; no agenesis corpus callosum
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00003202
0000002043
no coronal craniosynostosis (left/right); no cleft lip; no cleft palate; no duplex thumb/hallux
-
-
Familial
-
-
-
-
-
Johan den Dunnen
00003203
0000002044
coronal craniosynostosis left; cleft lip; cleft palate; duplex hallux left/right; partial agenesis corpus callosum; developmental delay
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00003204
0000002045
coronal craniosynostosis left; no cleft lip; no cleft palate; no duplex thumb/hallux; no agenesis corpus callosum; intracranial dermoid; double uterus
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00003205
0000002046
coronal craniosynostosis (left/right); cleft lip; cleft palate; no duplex thumb/hallux; no agenesis corpus callosum
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00003206
0000002047
coronal craniosynostosis left; no cleft lip; no cleft palate; no duplex thumb/hallux
-
-
Familial
-
-
-
-
-
Johan den Dunnen
00003207
0000002048
coronal craniosynostosis (left/right); no cleft lip; no cleft palate; duplex hallux right; no agenesis corpus callosum
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00003208
0000002049
coronal craniosynostosis right; no cleft lip; no cleft palate; no duplex thumb/hallux; partial agenesis corpus callosum; duplex left kidney
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00003209
0000002050
coronal craniosynostosis left; no cleft lip; no cleft palate; no duplex thumb/hallux; no agenesis corpus callosum; ulnar clinodactyly right middle finger
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00003210
0000002051
coronal craniosynostosis (left/right); no cleft lip; no cleft palate; no duplex thumb/hallux; no agenesis corpus callosum
-
-
Familial
-
-
-
-
-
Johan den Dunnen
00003211
0000002052
coronal craniosynostosis (left/right); no cleft lip; no cleft palate; no duplex thumb/hallux; no agenesis corpus callosum; cerebellar dysplasia; vesico-ureteric reflux
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00003212
0000002053
coronal craniosynostosis (left/right); no cleft lip; no cleft palate; no duplex thumb/hallux; no agenesis corpus callosum
-
-
Familial
-
-
-
-
-
Johan den Dunnen
00003213
0000002054
no coronal craniosynostosis (left/right); no cleft lip; no cleft palate; duplex hallux left; partial agenesis corpus callosum; developmental delay
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00003214
0000002055
coronal craniosynostosi; cleft lip; cleft palate; no duplex thumb/hallux; no agenesis corpus callosum; diaphragmatic hernia; sacrococcygeal teratoma (son)
-
-
Familial
-
-
-
-
-
Johan den Dunnen
00003215
0000002056
coronal craniosynostosis right; no cleft lip; cleft palate; no duplex thumb/hallux; no agenesis corpus callosum
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00003216
0000002057
-
-
-
Familial
-
-
-
-
-
Johan den Dunnen
00003217
0000002058
no cleft lip; no cleft palate; no duplex thumb/hallux; agenesis corpus callosum; developmental delay
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00003218
0000002059
coronal craniosynostosis right; no cleft lip; no cleft palate; no duplex thumb/hallux; no agenesis corpus callosum
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00003219
0000002060
coronal craniosynostosi; no cleft lip; no cleft palate; no duplex thumb/hallux; no agenesis corpus callosum
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00003220
0000002061
coronal craniosynostosis left; no cleft lip; no cleft palate; no duplex thumb/hallux; no agenesis corpus callosum; diaphragmatic hernia right
-
-
Familial
-
-
-
-
-
Johan den Dunnen
00003221
0000002062
coronal craniosynostosis right; no cleft lip; no cleft palate; no duplex thumb/hallux; no agenesis corpus callosum; bilateral dysplastic hips
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00003222
0000002063
coronal craniosynostosis left; no cleft lip; no cleft palate; no duplex thumb/hallux; partial agenesis corpus callosum; mother bicornuate uterus
-
-
Familial
-
-
-
-
-
Johan den Dunnen
00003223
0000002064
coronal craniosynostosis right; no cleft lip; no cleft palate; no duplex thumb/hallux; agenesis corpus callosum; sensorineural hearing loss
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00003224
0000002065
coronal craniosynostosis (left/right); no cleft lip; no cleft palate; no duplex thumb/hallux; agenesis corpus callosum
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00003225
0000002066
coronal craniosynostosis right; no cleft lip; no cleft palate; no duplex thumb/hallux; no agenesis corpus callosum
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00003226
0000002067
coronal craniosynostosis left; no cleft lip; no cleft palate; no duplex thumb/hallux; developmental delay
-
-
Familial
-
-
-
-
-
Johan den Dunnen
00003227
0000002073
hypertelorism, craniofacial abnormalities (orbital asymmetry), normal mental performance, no behavioral abnormalitiesnormal body height; III1-hypertelorism, bifid nasal tip, grooved nails, axillary pterygium, slight pterygium colli; I2/II6, hypertelorism, grooved nails; male carriers II3/II5 hypertelorism
-
-
Familial, X-linked dominant, male sparing
-
-
-
-
-
Johan den Dunnen
00003233
0000002074
hypertelorism, orbital asymmetry, brachycephaly, brachydactyly, Sprengel deformity, normal mental performance, no behavioral abnormalitiesnormal body height; III6 had four miscarriages (mid-pregnancy), uterus arcuatus, curly hair, grooved finger nails, unilateral breast hypoplasia; III2 (male) phenotypic abnormalities; V3 (male) broad nasal bridge (9y inner canthel distance 3.8 cm)
-
-
Familial, X-linked dominant, male sparing
-
-
-
-
-
Johan den Dunnen
00003234
0000002075
normal mental performance, no behavioral abnormalitiesnormal body height; I1 (male) slight facial asymmetry, broad nasal bridge; II1 severe facial asymmetry, hypertelorism, hypoplasia corpus callosum; III2 facial asymmetry, hypertelorism, agenesis corpus callosum, complete syndactyly left 3/4th finger, scoliosis
-
-
Familial, X-linked dominant, male sparing
-
-
-
-
-
Johan den Dunnen
00003235
0000017669
-
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019820
0000049865
coronal craniosynostosis R (HP:0004440), hypertelorism (HP:0000316), grooved nasal tip (HP:0000456), no down slanting palpebral fissures (-HP:0000494), unilateral cleft lip (HP:0100333), cleft palate (HP:0000175), no agenesis corpus callosum (-HP:0001274), mild learning disability (HP:0001328), no Sprengel deformity (-HP:0000912), grooved nails (HP:0001807), no brachydactyly (-HP:0001156), syndactyly 2nd-3rd toes L (HP:0004691), no clinodactyly (-HP:0030084), no low set ears (-HP:0000369), wiry hair, ptosis (HP:0000508), no undescended testes (-HP:0000028), small ASD-resolved spontaneously, sloping shoulders, umbilical hernia (HP:0001537)
-
-
Familial, X-linked
-
-
-
-
-
Johan den Dunnen
00003114
0000049866
coronal craniosynostosis R/L (HP:0004440), hypertelorism (HP:0000316), grooved nasal tip (HP:0000456), nodown slanting palpebral fissures (HP:0000494), high arched palate (HP:0002705), agenesis corpus callosum (HP:0001274), mild learning disability (HP:0001328), Sprengel deformity (HP:0000912), grooved nails (HP:0001807), brachydactyly (-HP:0001156) delta phalanx digit one right hand, syndactyly 2nd-3rd toes L (HP:0004691), no clinodactyly (-HP:0030084), low set ears (-HP:0000369), no wiry hair, ptosis (HP:0000508) left eye only, undescended testes R/L (HP:0000028), mild pectus excavatum, duplication of distal phalanx R thumb, postaxial polydactyly type B R hand, R inguinal hernia
-
-
Familial, X-linked
-
-
-
-
-
Johan den Dunnen
00003117
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