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

 Phenotype ID
|

 Diagnosis/Initial
|

 Diagnosis/Definite
|

 Phenotype details
|

 Inheritance
|

 Age/Examination
|

 Age/Diagnosis
|

 Age/Onset
|

 Phenotype/Onset
|

 Owner
|

 Individual ID
|
0000227027 |
ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299714 |
0000227028 |
ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299715 |
0000227029 |
ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299716 |
0000227030 |
ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299717 |
0000227031 |
ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299718 |
0000227032 |
ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299719 |
0000227033 |
ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299720 |
0000227034 |
ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299721 |
0000227035 |
ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299722 |
0000227036 |
ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299723 |
0000227037 |
ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299724 |
0000227038 |
ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299725 |
0000227039 |
ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299726 |
0000227040 |
ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299727 |
0000227041 |
ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299728 |
0000227042 |
ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299729 |
0000227043 |
hypohidrotic ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299730 |
0000227044 |
hypohidrotic ectodermal dysplasia |
XHED |
- |
Isolated (sporadic) |
- |
- |
- |
- |
Johan den Dunnen |
00299731 |
0000227045 |
hypohidrotic ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299732 |
0000227046 |
hypohidrotic ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299733 |
0000227047 |
hypohidrotic ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299734 |
0000227048 |
hypohidrotic ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299735 |
0000227049 |
hypohidrotic ectodermal dysplasia |
XHED |
- |
Isolated (sporadic) |
- |
- |
- |
- |
Johan den Dunnen |
00299736 |
0000227050 |
hypohidrotic ectodermal dysplasia |
XHED |
- |
Isolated (sporadic) |
- |
- |
- |
- |
Johan den Dunnen |
00299737 |
0000227051 |
hypohidrotic ectodermal dysplasia |
XHED |
- |
Isolated (sporadic) |
- |
- |
- |
- |
Johan den Dunnen |
00299738 |
0000227052 |
hypohidrotic ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299739 |
0000227053 |
hypohidrotic ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299740 |
0000227054 |
hypohidrotic ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299741 |
0000227055 |
hypohidrotic ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299742 |
0000227056 |
hypohidrotic ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299743 |
0000227057 |
hypohidrotic ectodermal dysplasia |
XHED |
- |
Isolated (sporadic) |
- |
- |
- |
- |
Johan den Dunnen |
00299744 |
0000227058 |
hypohidrotic ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299745 |
0000227059 |
hypohidrotic ectodermal dysplasia |
XHED |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
Johan den Dunnen |
00299746 |
0000227060 |
anhidrotic ectodermal dysplasia |
XHED |
recurrent fever 38oC due to the absence of sweating since birth, characteristic facial appearance, anhidrosis; 1m- eruptions on face and head spread to entire body; diagnosed with atopic dermatitis, nasal allergy, chronic sinusitis, heat intolerance; fine curly sparse hair, absent eyebrows, saddle nose, conical teeth, deciduous canine and second premolar teeth, permanent first incisor and first molar teeth maxillary ridge, no deciduous and permanent tooth buds in mandible |
Familial, X-linked recessive |
10y |
- |
- |
- |
Johan den Dunnen |
00299747 |
0000227149 |
hypohidrotic ectodermal dysplasia |
ECTD11 |
- |
Familial |
- |
- |
- |
- |
Johan den Dunnen |
00299828 |
0000227150 |
hypohidrotic ectodermal dysplasia |
ECTD11 |
- |
Familial |
- |
- |
- |
- |
Johan den Dunnen |
00299829 |
0000227151 |
hypohidrotic ectodermal dysplasia |
ECTD11 |
- |
Familial |
- |
- |
- |
- |
Johan den Dunnen |
00299830 |
0000279724 |
ectodermal dysplasia |
- |
ectodermal dysplasia |
Unknown |
11y |
- |
- |
- |
Johan den Dunnen |
00385921 |
0000292412 |
anhidrotic ectodermal dysplasia |
ECTD11B |
see paoer; ..., severe hypo-hidrotic and anhidrotic ectodermal dysplasia, multiple pulmonary infections; sparse hair, oligodontia with conical widely spaced teeth, ichthyosiform dry skin, prominent lips, frontal bossing, pointed chin; inability to sweat, episodes severe hyperpyrexia since early childhood |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00399295 |
0000292448 |
ectodermal dysplasia |
XHED |
hypotrichosis; anhidrosis; normal nails; severe oligodontia, conical incisors; facila dysmorphism, hyperkeratosis |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00399331 |
0000292449 |
ectodermal dysplasia |
XHED |
hypotrichosis; hypohidrosis, skin severe dryness; normal nails; oligodontia, conical incisors; facila dysmorphism |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00399332 |
0000292450 |
ectodermal dysplasia |
XHED |
hypotrichosis; hypohidrosis, dry skin; normal nails; oligodontia, conical incisors; facila dysmorphism |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00399333 |
0000292451 |
ectodermal dysplasia |
XHED |
hypotrichosis; normal skin; normal nails; oligodontia, tapered incisors; facila dysmorphism |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00399334 |
0000292452 |
ectodermal dysplasia |
XHED |
hypotrichosis; anhidrosis, skin severe dryness; spoon-shaped nails; severe oligodontia, conical incisors; facila dysmorphism |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00399335 |
0000292453 |
ectodermal dysplasia |
XHED |
hypotrichosis; anhidrosis, skin severe dryness; normal nails; severe oligodontia, conical incisors; facila dysmorphism |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00399336 |
0000292454 |
ectodermal dysplasia |
ECTD10B |
hypotrichosis; dry skin; normal nails; severe oligodontia, conical incisors; facila dysmorphism, palmar hyperhidrosis |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00399337 |
0000292455 |
ectodermal dysplasia |
ECTD10B |
hypotrichosis; anhidrosis, dry skin; normal nails; severe oligodontia, conical incisors, class III malocclusion; facila dysmorphism, psychomotor retardation |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00399338 |
0000292456 |
ectodermal dysplasia |
ECTD10B |
hypotrichosis; hypohidrosis, , skin severe dryness; normal nails; severe oligodontia, conical incisors, class III malocclusion; facila dysmorphism, palmar hyperhidrosis |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00399339 |
0000292457 |
ectodermal dysplasia |
ECTD10B |
hypotrichosis; hypohidrosis; spoon-shaped nails; severe oligodontia, conical incisors; facila dysmorphism, clinodactyly, postaxial polydactyly |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00399340 |
0000292458 |
ectodermal dysplasia |
ECTD10B |
hypotrichosis; anhidrosis, dry skin; normal nails; severe oligodontia, conical incisors; facila dysmorphism |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00399341 |
0000292459 |
ectodermal dysplasia |
ECTD10B |
hypotrichosis; hypohidrosis; spoon-shaped nails; severe oligodontia, conical incisors; facila dysmorphism |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00399342 |
0000292460 |
ectodermal dysplasia |
ECTD11B |
hypotrichosis; anhidrosis, dry skin; spoon-shaped nails; severe oligodontia, class III malocclusion; facila dysmorphism, blue sclera, palmar hyperhidrosis |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00399343 |
0000292461 |
ectodermal dysplasia |
ECTD11B |
hypotrichosis; hypohidrosis, dry skin; spoon-shaped nails; severe oligodontia, class III malocclusion; facila dysmorphism, palmar keratosis |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00399344 |
0000292462 |
ectodermal dysplasia |
- |
hypotrichosis; hypohidrosis, dry skin; normal nails; oligodontia; |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00399345 |
0000292463 |
ectodermal dysplasia |
- |
hypotrichosis; hypohidrosis, skin severe dryness; normal nails; severe oligodontia, tapered incisors (only permanant teeth); |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00399346 |
0000292464 |
ectodermal dysplasia |
- |
hypotrichosis; hypohidrosis, dry skin; normal nails; severe oligodontia, tapered incisors (only permanant teeth); |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00399347 |
0000292465 |
ectodermal dysplasia |
- |
hypotrichosis; dry skin; spoon-shaped nails; severe oligodontia, conical incisors, class III malocclusion; Palmar hyperhidrosis |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00399348 |
0000292466 |
ectodermal dysplasia |
- |
hypotrichosis; hypohidrosis, dry skin; spoon-shaped nails; severe oligodontia (only permanant teeth); atopic dermatitis |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00399349 |
0000333183 |
ectodermal dysplasia |
ECTD4 |
see paper; ..., ectodermal dysplasia of hair and nail type; total alopecia, nail dystrophy since birth, hairs absent from scalp, face, chest, arms, legs; born completely devoid of eyebrows and eyelashes, never developed axillary and pubic hair |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00443920 |