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

 Phenotype ID
|

 Phenotype details
|

 Diagnosis/Initial
|

 Diagnosis/Definite
|

 Inheritance
|

 Age/Examination
|

 Age/Diagnosis
|

 Age/Onset
|

 Phenotype/Onset
|

 Protein
|

 Owner
|

 Individual ID
|
| 0000025737 |
scalp defect; TTLD of hands and feet; microcephaly; developmental delay; |
- |
- |
Familial, autosomal recessive |
03y06m |
- |
- |
- |
- |
Maja Sukalo |
00029773 |
| 0000025738 |
scalp defect; TTLD of hands and feet; aortic valve dysplasia; ventricular dilatation / brain atrophy; periventricular lesions (calcification, gliosis); abdominal skin defect; |
- |
- |
Familial, autosomal recessive |
01y00m |
- |
- |
- |
- |
Maja Sukalo |
00029774 |
| 0000025739 |
scalp defects; TTLD of hands and feet; ventricular dilatation / brain atrophy; periventricular lesions (calcification, gliosis); seizures / epilepsy; gastroschisis; |
- |
- |
Familial, autosomal recessive |
? |
- |
- |
- |
- |
Maja Sukalo |
00029775 |
| 0000025740 |
scalp defect; TTLD of hands and feet; periventricular lesions (calcification, gliosis); pachygyria; optic atrophy; seizures / epilepsy; |
- |
- |
Familial, autosomal recessive |
02y00m |
- |
- |
- |
- |
Maja Sukalo |
00029776 |
| 0000025741 |
IUGR; scalp defect; TTLD of hands and feet; tetralogy of Fallot; persistent left superior vena cava; periventricular lesions (calcification, gliosis); porencephaly; microcephaly; retinal detachment; severe ID; seizures / epilepsy; placental vasculopathy; neonatal thrombocytopenia; small bowel infarction; |
- |
- |
Familial, autosomal recessive |
02y00m |
- |
- |
- |
- |
Maja Sukalo |
00029777 |
| 0000025742 |
scalp defect; TTLD of hands and feet; microcephaly; microphthalmia; retinal detachment; vitreous opacities/membranes; anterior chamber abnormality; developmental delay; seizures / epilepsy; high palate; |
- |
- |
Familial, autosomal recessive |
05y00m |
- |
- |
- |
- |
Maja Sukalo |
00029778 |
| 0000025743 |
scalp defect; TTLD of hands and feet; ventricular dilatation / brain atrophy; corpus callosum hypoplasia/atrophy; microcephaly; ocular anomaly; severe ID; seizures / epilepsy; cerebral palsy / spasticity; CMTC; single umbilical artery; cryptorchidism; |
- |
- |
Familial, autosomal recessive |
10y00m |
- |
- |
- |
- |
Maja Sukalo |
00029779 |
| 0000025744 |
IUGR; scalp defect; TTLD of hands and feet; ventricular dilatation / brain atrophy; periventricular lesions (calcification, gliosis); microcephaly; microphthalmia; retinal detachment; anterior chamber abnormality; severe ID; seizures / epilepsy; cerebral palsy / spasticity; CMTC; abdominal skin defect; |
- |
- |
Familial, autosomal dominant |
20y00m |
- |
- |
- |
- |
Maja Sukalo |
00029780 |
| 0000025745 |
scalp defect; TTLD of hands and feet; patent ductus arteriosus; ventricular dilatation / brain atrophy; microcephaly; microphthalmia; knee dislocation; |
- |
- |
Familial, autosomal recessive |
00y03m |
- |
- |
- |
- |
Maja Sukalo |
00029781 |
| 0000025746 |
IUGR; scalp defect; TTLD of hands and feet; ventricular dilatation / brain atrophy; corpus callosum hypoplasia/atrophy; periventricular lesions (calcification, gliosis); microcephaly; microphthalmia; retinal detachment; moderate ID; seizures / epilepsy; cryptorchidism; |
- |
- |
Familial, autosomal recessive |
09y00m |
- |
- |
- |
- |
Maja Sukalo |
00029782 |
| 0000025747 |
scalp defect; TTLD of hands and feet; ventricular septal defect; ventricular dilatation / brain atrophy; periventricular lesions (calcification, gliosis); microcephaly; microphthalmia; retinal detachment; vitreous opacities/membranes; severe ID; seizures / epilepsy; cerebral palsy / spasticity; abdominal skin defects; absence of right patella; |
- |
- |
Familial, autosomal recessive |
? |
- |
- |
- |
- |
Maja Sukalo |
00029783 |
| 0000025748 |
IUGR; scalp defects; TTLD of hands and feet; ventricular dilatation / brain atrophy; corpus callosum hypoplasia/atrophy; retinal detachment; abdominal skin defect; patella fixed to skin; |
- |
- |
Familial, autosomal recessive |
00y00m |
- |
- |
- |
- |
Maja Sukalo |
00029784 |
| 0000025749 |
scalp defect; TTLD of hands and feet; brain anomalies; microcephaly; ocular anomalies; severe ID; seizures / epilepsy; abdominal skin defect; |
- |
- |
Familial, autosomal recessive |
07y00m |
- |
- |
- |
- |
Maja Sukalo |
00029785 |
| 0000025750 |
IUGR; TTLD of feet; total anomalous pulmonary venous connection; ocular anomalies; mild ID; hypothyroidism; |
- |
- |
Familial, autosomal recessive |
08y00m |
- |
- |
- |
- |
Maja Sukalo |
00029786 |
| 0000025751 |
scalp defect; TTLD of hands and feet; no further data available; |
- |
- |
Familial, autosomal recessive |
? |
- |
- |
- |
- |
Maja Sukalo |
00029787 |
| 0000025752 |
scalp defect; TTLD of hands and feet; periventricular lesions (calcification, gliosis); no further data available; |
- |
- |
Familial, autosomal recessive |
07y00m |
- |
- |
- |
- |
Maja Sukalo |
00029788 |
| 0000025753 |
scalp defect; TTLD of hands and feet; ventricular dilatation / brain atrophy; corpus callosum hypoplasia/atrophy; periventricular lesions (calcification, gliosis); microcephaly; seizures / epilepsy; |
- |
- |
Familial, autosomal recessive |
? |
- |
- |
- |
- |
Maja Sukalo |
00029789 |
| 0000025754 |
scalp defect; TTLD of hands and feet; ventricular dilatation / brain atrophy; periventricular lesions (calcification, gliosis); microcephaly; optic atrophy; severe ID; seizures / epilepsy; cerebral palsy / spasticity |
- |
- |
Familial, autosomal recessive |
00y11m |
- |
- |
- |
- |
Maja Sukalo |
00029772 |
| 0000025756 |
see paper; .. |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Johan den Dunnen |
00029791 |
| 0000025757 |
- |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Johan den Dunnen |
00029792 |
| 0000025774 |
see paper; syndactyly 2nd/3rd toes, otherwise normal, short palpebral fissures, mildly delayed gross motor milestones, microcephaly, aplasia cutis congenita scalp (HP:0007385) |
- |
- |
Familial, autosomal recessive |
00y00m00d |
- |
- |
- |
- |
Johan den Dunnen |
00029801 |
| 0000025775 |
see paper; shortened distal phalanges left hand, bilateral reduction toes, no intellectual disability |
- |
- |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00029802 |
| 0000025776 |
see paper; aplasia cutis congenita, bony defect/abnormal fontanelle, terminal transverse limb defects, syndactyly |
- |
- |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00029803 |
| 0000025777 |
see paper; aplasia cutis congenita, bony defect/abnormal fontanelle, terminal transverse limb defects, syndactyly |
- |
- |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00029804 |
| 0000025874 |
see paper; .. |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Johan den Dunnen |
00032397 |
| 0000027454 |
- |
- |
- |
Familial |
- |
- |
- |
- |
- |
Maja Sukalo |
00034059 |
| 0000027457 |
- |
- |
- |
Familial |
- |
- |
- |
- |
- |
Maja Sukalo |
00034062 |
| 0000027458 |
- |
- |
- |
Familial |
- |
- |
- |
- |
- |
Maja Sukalo |
00034063 |
| 0000027459 |
- |
- |
- |
Familial |
- |
- |
- |
- |
- |
Maja Sukalo |
00034064 |
| 0000027460 |
- |
- |
- |
Familial |
- |
- |
- |
- |
- |
Maja Sukalo |
00034065 |
| 0000027461 |
- |
- |
- |
Familial |
- |
- |
- |
- |
- |
Maja Sukalo |
00034066 |
| 0000027462 |
- |
- |
- |
Familial |
- |
- |
- |
- |
- |
Maja Sukalo |
00034067 |
| 0000027463 |
- |
- |
- |
Familial |
- |
- |
- |
- |
- |
Maja Sukalo |
00034068 |
| 0000027464 |
- |
- |
- |
Familial |
- |
- |
- |
- |
- |
Maja Sukalo |
00034069 |
| 0000027465 |
- |
- |
- |
Familial |
- |
- |
- |
- |
- |
Maja Sukalo |
00034070 |
| 0000027466 |
- |
- |
- |
Familial |
- |
- |
- |
- |
- |
Maja Sukalo |
00034071 |
| 0000027467 |
- |
- |
- |
Familial |
- |
- |
- |
- |
- |
Maja Sukalo |
00034072 |
| 0000027468 |
- |
- |
- |
Familial |
- |
- |
- |
- |
- |
Maja Sukalo |
00034073 |
| 0000027469 |
- |
- |
- |
Familial |
- |
- |
- |
- |
- |
Maja Sukalo |
00034074 |
| 0000036656 |
no further details, aplasia cutis congenita scalp (HP:0007385) |
- |
- |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Johan den Dunnen |
00049883 |
| 0000036657 |
short distal phalangus middle finger right hand, symphalangism index finger, symbrachydactyly both feet; truncus arteriosus, ventricular septum defect; growth hormone deficiency, aplasia cutis congenita scalp (HP:0007385) |
- |
- |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Johan den Dunnen |
00049882 |
| 0000036668 |
no further details, aplasia cutis congenita scalp (HP:0007385) |
- |
- |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Johan den Dunnen |
00049877 |
| 0000036670 |
left brachydactyly 3rd4th toes (confirmed by X-ray), normal scalp |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00049874 |
| 0000036671 |
short distal phalanges (not confirmed by X-ray), normal scalp |
- |
- |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00049893 |
| 0000036672 |
normal echocardiogram, aplasia cutis congenita scalp (HP:0007385) |
- |
- |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00049894 |
| 0000036673 |
brachydactyly, syndactyly 2nd/3rd toes right foot; tricuspid insufficiency, ventricular septum defect, aplasia cutis congenita scalp (HP:0007385) |
- |
- |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00049895 |
| 0000036674 |
ACC with underlying skull defect; brachydactyly left foot, missing toes right foot; normal echocardiogram, aplasia cutis congenita scalp (HP:0007385) |
- |
- |
Familial |
- |
- |
- |
- |
- |
Johan den Dunnen |
00049896 |
| 0000036675 |
ACC with underlying skull defect; brachysyndactyly right foot, severe
brachysyndactyly left foot; normal echocardiogram; small kidneys, mild hypertension, aplasia cutis congenita scalp (HP:0007385) |
- |
- |
Familial |
- |
- |
- |
- |
- |
Johan den Dunnen |
00049897 |
| 0000036676 |
, aplasia cutis congenita scalp (HP:0007385) |
- |
- |
Familial |
- |
- |
- |
- |
- |
Johan den Dunnen |
00049876 |
| 0000036677 |
, aplasia cutis congenita scalp (HP:0007385) |
- |
- |
Familial |
- |
- |
- |
- |
- |
Johan den Dunnen |
00049898 |
| 0000036678 |
syndactyly 2nd/3rd toes, hypoplastic toe nails, brachydactyly toes |
- |
- |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00049878 |
| 0000036679 |
bald area on scal, cutis marmorata |
- |
- |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00049900 |
| 0000036680 |
bald area on scalp; brachydactyly fingers/toes, syndactyly 2nd/3rd toes |
- |
- |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00049901 |
| 0000036681 |
bald area on scalp |
- |
- |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00049903 |
| 0000036682 |
ACC with underlying skull defect, aplasia cutis congenita scalp (HP:0007385) |
- |
- |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00049904 |
| 0000036683 |
normal echocardiogram; cutis marmorata, epilepsy, learning difficulties,
borderline intellectual function (TIQ 76) at young age, normal IQ at later age; mild periventricular leukomalacia, aplasia cutis congenita scalp (HP:0007385) |
- |
- |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00049905 |
| 0000036684 |
normal echocardiogram, portal hypertension; esophageal varices splenomegaly, congenital liver fibrosis, aplasia cutis congenita scalp (HP:0007385) |
- |
- |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00049906 |
| 0000036685 |
no cardiac problems, no dilatation, aplasia cutis congenita scalp (HP:0007385) |
- |
- |
Familial |
- |
- |
- |
- |
- |
Johan den Dunnen |
00049879 |
| 0000036686 |
normal echocardiogram, aplasia cutis congenita scalp (HP:0007385) |
- |
- |
Familial |
- |
- |
- |
- |
- |
Johan den Dunnen |
00049907 |
| 0000036687 |
delayed ossification; hypoplastic toe nails; no cardiac problems; cutis marmorata; 2m-normal chest X-ray, aplasia cutis congenita scalp (HP:0007385) |
- |
- |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Johan den Dunnen |
00049908 |
| 0000244360 |
stroke, abnormal cerebral morphology, leukoencephalopathy, vasculitis, abnormality of lysosomal metabolism, inflammatory arteriopathy, recurrent subcortical infarcts, abnormal cerebral artery morphology, abnormality of the cerebral subcortex, abnormal cellular physiology, abnormality of the cerebral vasculature |
- |
- |
Unknown |
48y |
- |
- |
- |
- |
Andreas Laner |
00325873 |