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Phenotypes for disease #05171 (CSCSC1 (skin crease, circumferential, symmetric, congenital, type 1 (CSCSC-1, Kunze type)), OMIM:156610)
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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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Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000051856
no decreased head circumference present at birth (-HP:0011451), no reduced head circumference – current (-HP:0000252), cleft palate (HP:0000175), creases limbs (HP:?), creases neck (HP:?), flat face (HP:0012368), microphthalmia (HP:0000568), short palpebral fissures (HP:0012745), epicanthal folds (HP:0000286), low broad nasal bridge (-HP:0000431), lowset (HP:0000369), small dysplastic ears (HP:0000377), hypoplastic scrotum (HP:0000046), coronal hypospadias (HP:0008743), intellectual disability, moderate (HP:0002342) to intellectual disability, severe (HP:0010864), mildly dilated lateral ventricles (HP:0006956), corpus callosum hypoplasia (HP:0002079), seizures (HP:0001250)
-
-
Familial, autosomal recessive
00y15m
-
-
-
-
Jamie Zeegers
00072150
0000051857
decreased head circumference present at birth (HP:0011451), reduced head circumference – current (HP:0000252), cleft palate (HP:0000175), creases limbs (HP:?), elongated face (HP:0000300), hypertelorism (HP:0000316), bilateral epicanthic folds (HP:0000286), upslanting palpebral fissures (HP:0000582), microphthalmia (HP:0000568), strabismus (HP:0000486), wide nasal bridge (HP:0000431), aberrant teeth (HP:0006482), low-set posteriorly rotated ears (HP:0000368) with overfolded thick helices (HP:0000391), short neck (HP:0000470), widely spaced nipples (HP:0006610), hypospadias (HP:0000047), undescended testes (HP:0000028), second and third toe syndactyly (HP:0004691), intellectual disability, moderate (HP:0002342), unable to walk (HP:0002540), unable to speak (HP:0002371), hypoplastic vermis (HP:0001320), hypoplastic corpus callosum (HP:0002079), mild dilatation of ventricles (HP:0006956), deafness (HP:0000365), seizures (HP:0001250) and ureterocele with vesical reflux (HP:0008714 ) without impairment of the renal function (-HP:0012622)
-
-
Familial, autosomal recessive
19y
-
-
-
-
Jamie Zeegers
00072151
0000051858
decreased head circumference present at birth (HP:0011451), reduced head circumference – current (HP:0000252), creases limbs; disappeared around age 4 years (HP:?), no cleft palate (-HP:0000175), flat face (HP:0012368), low set anterior hairline (HP:0000294), microphthalmia (HP:0000568), bilateral epicanthic folds (HP:0000286), small downslanting palpebral fissures (HP:0000494), ptosis (HP:0000508), synophris (HP:0000664), broad nasal bridge (HP:0000431), dysplastic small (HP:0000377), low-set and posteriorly rotated ears (HP:0000368) with overfolded helices (HP:0000396), upturned ear lobes (HP:0009909); microstomia (HP:0000160)with thin upper lip (HP:0000219), small chin (HP:0000331), short hands (HP:0004279), tapering fingers (HP:0001182), intellectual disability, mild (HP:0001256) to normal
-
-
Isolated (sporadic)
08y09m
-
-
-
-
Jamie Zeegers
00072152
0000051859
decreased head circumference present at birth (HP:0011451), reduced head circumference – current (HP:0000252), cleft palate (HP:0000175), limbs; spontaneous improvement (HP:?), microphthalmia (HP:0000568) with small upslanting palpebral fissures (HP:0000582), epicanthal folds (HP:0000286), broad nasal bridge (HP:0000431), flat midface (HP:0040199), small mouth (HP:0000160), small chin (HP:0000331), clinodactyly of fifth fingers (HP:0004209), intellectual disability, mild (HP:0001256) to intellectual disability, moderate (HP:0002342)
-
-
Familial, autosomal recessive
06y
-
-
-
-
Jamie Zeegers
00072153
0000051860
decreased head circumference present at birth (HP:0011451), reduced head circumference – current (HP:0000252), cleft palate (HP:0000175), creases limbs: fingers, neck, penis – improved at follow-up, but visible (HP:?), microphthalmia (HP:0000568), short palpebral fissures (HP:0012745), epicanthal folds (HP:0000286), flat supraorbital ridge (HP:0009891), low nasal bridge (HP:0005280), long philtrum (HP:0000343), small mouth (HP:0000160), small low-set posteriorly rotated malformed (HP:0000377) ears (HP:0000368) with thick overfolded helices (HP:0000396), brachycephaly (HP:0000248), wide-spaced nipples (HP:0006610), intellectual disability, mild (HP:0001256), normal brain imaging (HP:?)
-
-
Isolated (sporadic)
15y
-
-
-
-
Jamie Zeegers
00072155
0000051862
no decreased head circumference present at birth (HP:0011451), reduced head circumference – current (HP:0000252), cleft palate (HP:0000175), creases limbs and neck; disappeared at age 4 years; still creases on wrists (HP:?), short palpebral fissures (HP:0012745), blepharophimosis (HP:0000581, broad nasal bridge (HP:0000431) with epicanthal folds (HP:0000286), flat face (HP:0012368), small mouth (HP:0000160), mild asymmetry in face and abdomen (HP:?), low-set dysmorphic and posteriorly rotated ears (HP:0000368), short neck (HP:0000470), long fingers (HP:0100807), intellectual disability, mild (HP:0001256) to intellectual disability, moderate (HP:0002342), normal brain imaging (HP:?), infantile hypotonia (HP:0008947)
-
-
Isolated (sporadic)
05y06m
-
-
-
-
Jamie Zeegers
00072156
0000051863
reduced head circumference – current (HP:0000252), high palate (HP:0000218), no cleft palate (-HP:0000175), creases limbs (HP:?), elongated face (HP:0000300), flat face (HP:0012368), hypertelorism (HP:0000316), upslanting short palpebral fissures (HP:0000582), epicanthus (HP:0000286), periorbital fullness (HP:0000629), long eyelashes (HP:0000527), blepharophimosis (HP:0000581), broad nasal bridge (HP:0000431), depressed nasal bridge (HP:0005280), malformed ears (HP:0000377 ), lowset ears (HP:0000369), microstomia (HP:0000160), down-turned corners of the mouth (HP:0002714), wide-spaced nipples (HP:0006610), second and third toe syndactyly (HP:0004691), mild developmental delay (HP:0011342), particularly speech delay (HP:0000750), hypoplasia of corpus callosum (HP:0002079), Dandy-Walker malformation (HP:0001305)
-
-
Isolated (sporadic)
00y18m
-
-
-
-
Jamie Zeegers
00072157
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