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
Protein: result from protein staining

 Phenotype ID
|

 Diagnosis/Initial
|

 Diagnosis/Definite
|

 Phenotype details
|

 Inheritance
|

 Age/Examination
|

 Age/Diagnosis
|

 Age/Onset
|

 Phenotype/Onset
|

 Protein
|

 Owner
|

 Individual ID
|
0000326856 |
congenital diaphragmatic hernia |
- |
see paper; ..., deceased; congenital diaphragmatic hernia (unspecified) |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436743 |
0000326857 |
congenital diaphragmatic hernia |
- |
see paper; ..., alive; no diaphragm defect type; no body-wall defect; hypertelorism; no neurodevelopmental features |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436744 |
0000326858 |
congenital diaphragmatic hernia |
- |
see paper; ..., alive; no diaphragm defect type; supraumbilical abdominal hernia; hypertelorism; no neurodevelopmental features; high bone densitometry, genu valgum |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436745 |
0000326859 |
congenital diaphragmatic hernia |
- |
see paper; ..., alive; no diaphragm defect type; no body-wall defect; hypertelorism; no neurodevelopmental features |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436746 |
0000326860 |
congenital diaphragmatic hernia |
- |
see paper; ..., deceased; congenital diaphragmatic hernia (unspecified) |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436747 |
0000326861 |
congenital diaphragmatic hernia |
- |
see paper; ..., alive; no diaphragm defect type; hypertelorism; no neurodevelopmental features |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436748 |
0000326862 |
congenital diaphragmatic hernia |
- |
see paper; ..., alive; no diaphragm defect type; no body-wall defect; hypertelorism; no neurodevelopmental features |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436749 |
0000326863 |
congenital diaphragmatic hernia |
- |
see paper; ..., alive; no diaphragm defect type; supraumbilical abdominal hernia; hypertelorism; no neurodevelopmental features |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436750 |
0000326864 |
congenital diaphragmatic hernia |
- |
see paper; ..., alive; no diaphragm defect type; supraumbilical abdominal hernia; hypertelorism; no neurodevelopmental features |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436751 |
0000326865 |
congenital diaphragmatic hernia |
- |
see paper; ..., deceased; left congenital diaphragmatic hernia; omphalocele; dextrocardia |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436752 |
0000326866 |
congenital diaphragmatic hernia |
- |
see paper; ..., alive; no diaphragm defect type; no body-wall defect; hypertelorism; no neurodevelopmental features |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436753 |
0000326867 |
congenital diaphragmatic hernia |
- |
see paper; ..., deceased; diaphragm agenesis; no body-wall defect; neonatal seizures; bilateral renal pelvis dilation |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436754 |
0000326868 |
congenital diaphragmatic hernia |
- |
see paper; ..., alive; no diaphragm defect type; hypertelorism; no neurodevelopmental features |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436755 |
0000326869 |
congenital diaphragmatic hernia |
- |
see paper; ..., alive; congenital diaphragmatic hernia (unspecified); hypertelorism; intellectual disability |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436756 |
0000326870 |
congenital diaphragmatic hernia |
- |
see paper; ..., alive; congenital diaphragmatic hernia (unspecified); intellectual disability |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436757 |
0000326871 |
congenital diaphragmatic hernia |
- |
see paper; ..., deceased; left diaphragm agenesis; no body-wall defect; hypertelorism; hypotonia; left lung segmentation defect, bicuspid aortic valve, two choroid cysts |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436758 |
0000326872 |
congenital diaphragmatic hernia |
- |
see paper; ..., deceased (termination of pregnancy); left diaphragm agenesis; cystic hygroma, left lung segmentation defect |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436759 |
0000326873 |
congenital diaphragmatic hernia |
- |
see paper; ..., alive; no diaphragm defect type; umbilical hernia; no dysmorphic features; no neurodevelopmental features |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436760 |
0000326874 |
congenital diaphragmatic hernia |
- |
see paper; ..., deceased; left posterolateral congenital diaphragmatic hernia; supraumbilical abdominal muscle deficiency, cleft sternum; hypoplasia of corpus callosum |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436761 |
0000326875 |
congenital diaphragmatic hernia |
- |
see paper; ..., deceased; left diaphragm agenesis; supraumbilical abdominal muscle deficiency |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436762 |
0000326876 |
congenital diaphragmatic hernia |
- |
see paper; ..., alive; left posterolateral congenital diaphragmatic hernia; no body-wall defect; no dysmorphic features |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436763 |
0000326877 |
congenital diaphragmatic hernia |
- |
see paper; ..., deceased; no body-wall defect; left posterolateral congenital diaphragmatic hernia |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436764 |
0000326878 |
congenital diaphragmatic hernia |
- |
see paper; ..., alive; left posterolateral congenital diaphragmatic hernia; no body-wall defect; no dysmorphic features; hydronephrosis with ureteral abnormality |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436765 |
0000326879 |
congenital diaphragmatic hernia |
- |
see paper; ..., deceased; congenital diaphragmatic hernia (unspecified) |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436766 |
0000326880 |
congenital diaphragmatic hernia |
- |
see paper; ..., deceased; congenital diaphragmatic hernia (unspecified) |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436767 |
0000326881 |
congenital diaphragmatic hernia |
- |
see paper; ..., alive; congenital diaphragmatic hernia (unspecified); no neurodevelopmental features |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436768 |
0000326882 |
congenital diaphragmatic hernia |
- |
see paper; ..., alive; right congenital diaphragmatic hernia; absence of right-sided internal oblique and transversus abdominis muscles; no dysmorphic features; no neurodevelopmental features |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436769 |
0000326883 |
congenital diaphragmatic hernia |
- |
see paper; ..., alive; diaphragm eventration; no body-wall defect; no dysmorphic features; no neurodevelopmental features |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436770 |
0000326884 |
congenital diaphragmatic hernia |
- |
see paper; ..., alive; bilateral ventral CDH with hernia sacs; epigastric skin-covered abdominal-wall defect; hypertelorism, prominent forehead, broad flattened nasal bridge, downslanting palpebral fissures, low-set ears, micrognathia, anteverted nares; no neurodevelopmental features; membranous ventricular septal defect, atrial septal defect, hydronephrosis, unilateral cryptorchidism, unilateral inguinal hernia |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436771 |
0000326885 |
congenital diaphragmatic hernia |
- |
see paper; ..., deceased; congenital diaphragmatic hernia (unspecified) |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436772 |
0000326886 |
congenital diaphragmatic hernia |
- |
see paper; ..., deceased; congenital diaphragmatic hernia (unspecified) |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436773 |
0000326887 |
congenital diaphragmatic hernia |
- |
see paper; ..., alive; left congenital diaphragmatic hernia with hernia sac; no body-wall defect; hypertelorism, low-set right ear, short nose with wide nasal root, downslanting palpebral fissures, widely spaced teeth, high arched palate; intermittent horizontal nystagmus, dilation of lateral ventricles, speech delay, intellectual disability, autism, complex partial seizures; corneal pannus, sensory neural hearing loss, malocclusion, two-vessel umbilical cord |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00436774 |