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
How to query this table
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| Operator |
Column type |
Example |
Matches |
| |
Text |
Arg |
all entries containing 'Arg' |
| space |
Text |
Arg Ser |
all entries containing 'Arg' and 'Ser' |
| | |
Text |
Arg|Ser |
all entries containing 'Arg' or 'Ser' |
| ! |
Text |
!fs |
all entries not containing 'fs' |
| ^ |
Text |
^p.(Arg |
all entries beginning with 'p.(Arg' |
| $ |
Text |
Ser)$ |
all entries ending with 'Ser)' |
| ="" |
Text |
="" |
all entries with this field empty |
| ="" |
Text |
="p.0" |
all entries exactly matching 'p.0' |
| !="" |
Text |
!="" |
all entries with this field not empty |
| !="" |
Text |
!="p.0" |
all entries not exactly matching 'p.0?' |
| combination |
Text |
*|Ter !fs |
all entries containing '*' or 'Ter' but not containing 'fs' |
|
Date |
2020 |
all entries matching the year 2020 |
| | |
Date |
2020-03|2020-04 |
all entries matching March or April, 2020 |
| ! |
Date |
!2020-03 |
all entries not matching March, 2020 |
| < |
Date |
<2020 |
all entries before the year 2020 |
| <= |
Date |
<=2020-06 |
all entries in or before June, 2020 |
| > |
Date |
>2020-06 |
all entries after June, 2020 |
| >= |
Date |
>=2020-06-15 |
all entries on or after June 15th, 2020 |
| combination |
Date |
2019|2020 <2020-03 |
all entries in 2019 or 2020, and before March, 2020 |
|
Numeric |
23 |
all entries exactly matching 23 |
| | |
Numeric |
23|24 |
all entries exactly matching 23 or 24 |
| ! |
Numeric |
!23 |
all entries not exactly matching 23 |
| < |
Numeric |
<23 |
all entries lower than 23 |
| <= |
Numeric |
<=23 |
all entries lower than, or equal to, 23 |
| > |
Numeric |
>23 |
all entries higher than 23 |
| >= |
Numeric |
>=23 |
all entries higher than, or equal to, 23 |
| combination |
Numeric |
>=20 <30 !23 |
all entries with values from 20 to 29, but not equal to 23 |
Some more advanced examples:
| Example |
Matches |
| Asian |
all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc. |
| Asian !Caucasian |
all entries containing 'Asian' but not containing 'Caucasian' |
| Asian|African !Caucasian |
all entries containing 'Asian' or 'African', but not containing 'Caucasian' |
| "South Asian" |
all entries containing 'South Asian', but not containing 'South East Asian' |
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|
|
Legend |
How to query |

 Phenotype ID
|

 Phenotype details
|

 Diagnosis/Initial
|

 Diagnosis/Definite
|

 Inheritance
|

 Age/Examination
|

 Age/Diagnosis
|

 Age/Onset
|

 Phenotype/Onset
|

 Protein
|

 Owner
|

 Individual ID
|
| 0000237124 |
- |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Johan den Dunnen |
00311872 |
| 0000357098 |
see paper; ..., motor retardation; prominent forehead; brachycephaly; wide anterior fontanel; hypertelorism; congenital glaucoma; large cornea; prominent eyes; full cheeks; anteverted nostrils; broad mouth; broad alveolar ridges; micrognathia; protruding ears; kyphosis; prominent coccyx; bowing long bones; short hands; flexion deformity fingers; club feet; double right outlet |
Frank-Ter Haar syndrome |
FTHS |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Johan den Dunnen |
00472295 |
| 0000357099 |
see paper; ..., motor retardation; prominent forehead; brachycephaly; wide anterior fontanel; hypertelorism; congenital glaucoma; large cornea; prominent eyes; full cheeks; broad mouth; micrognathia; protruding ears; kyphosis; prominent coccyx; bowing long bones; short hands; no flexion deformity fingers; club feet; mitral valve anomaly |
Frank-Ter Haar syndrome |
FTHS |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Johan den Dunnen |
00472296 |
| 0000357100 |
see paper; ..., motor retardation; prominent forehead; brachycephaly; wide anterior fontanel; prominent eyes; full cheeks; anteverted nostrils; broad mouth; micrognathia; protruding ears; no kyphosis; prominent coccyx; bowing long bones; short hands; no flexion deformity fingers; no club feet; double right outlet |
Frank-Ter Haar syndrome |
FTHS |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Johan den Dunnen |
00472297 |
| 0000357101 |
see paper; ..., motor retardation; prominent forehead; brachycephaly; wide anterior fontanel; congenital glaucoma; large cornea; prominent eyes; micrognathia; kyphosis; flexion deformity fingers; club feet; mitral valve anomaly |
Frank-Ter Haar syndrome |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00472298 |
| 0000357102 |
see paper; ..., motor retardation; prominent forehead; brachycephaly; wide anterior fontanel; hypertelorism; no congenital glaucoma; large cornea; prominent eyes; full cheeks; anteverted nostrils; broad mouth; broad alveolar ridges; micrognathia; protruding ears; kyphosis; prominent coccyx; no bowing long bones; no short hands; flexion deformity fingers; no club feet; mitral valve prolapsed; no double right outlet; no ventricular septal defect |
Frank-Ter Haar syndrome |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00472299 |
| 0000357103 |
see paper; ..., motor retardation; prominent forehead; brachycephaly; wide anterior fontanel; hypertelorism; congenital glaucoma; large cornea; prominent eyes; full cheeks; anteverted nostrils; broad mouth; no broad alveolar ridges; micrognathia; kyphosis; bowing long bones; short hands; flexion deformity fingers; no club feet; ventricular septal defect |
Frank-Ter Haar syndrome |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00472300 |
| 0000357104 |
see paper; ..., motor retardation; prominent forehead; brachycephaly; wide anterior fontanel; hypertelorism; no congenital glaucoma; large cornea; prominent eyes; full cheeks; no anteverted nostrils; broad mouth; broad alveolar ridges; no micrognathia; protruding ears; no kyphosis; prominent coccyx; no bowing long bones; short hands; flexion deformity fingers; pes adductus; mitral valve anomaly; no double right outlet; ventricular septal defect; gall stones |
Frank-Ter Haar syndrome |
FTHS |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Johan den Dunnen |
00472301 |
| 0000357105 |
see paper; ..., motor retardation; prominent forehead; brachycephaly; wide anterior fontanel; hypertelorism; congenital glaucoma; large cornea; prominent eyes; full cheeks; anteverted nostrils; broad mouth; broad alveolar ridges; micrognathia; no protruding ears; prominent coccyx; bowing long bones; short hands; no flexion deformity fingers; club feet; no ventricular septal defect |
Frank-Ter Haar syndrome |
FTHS |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Johan den Dunnen |
00472302 |
| 0000357106 |
see paper; ..., motor retardation; prominent forehead; brachycephaly; wide anterior fontanel; hypertelorism; congenital glaucoma; large cornea; prominent eyes; full cheeks; anteverted nostrils; broad mouth; broad alveolar ridges; micrognathia; no protruding ears; prominent coccyx; bowing long bones; short hands; no flexion deformity fingers; club feet; ventricular septal defect |
Frank-Ter Haar syndrome |
FTHS |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Johan den Dunnen |
00472303 |
| 0000357107 |
see paper; ..., motor retardation; prominent forehead; no brachycephaly; wide anterior fontanel; hypertelorism; bilateral iris and retinal coloboma; no large cornea; prominent eyes; full cheeks; no anteverted nostrils; broad mouth; no broad alveolar ridges; micrognathia; no protruding ears; no kyphosis; prominent coccyx; no bowing long bones; no short hands; flexion deformity fingers; no club feet; no mitral valve anomaly; no double right outlet; no ventricular septal defect; MRI brain slightly prominent ventricles |
Frank-Ter Haar syndrome |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00472304 |
| 0000357108 |
see paper; ..., no motor retardation; prominent forehead; brachycephaly; wide anterior fontanel; hypertelorism; no congenital glaucoma; large cornea; prominent eyes; full cheeks; no anteverted nostrils; broad mouth; no broad alveolar ridges; micrognathia; kyphosis; no prominent coccyx; no bowing long bones; short hands; no flexion deformity fingers; no mitral valve anomaly; no ventricular septal defect |
Frank-Ter Haar syndrome |
FTHS |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Johan den Dunnen |
00472305 |
| 0000357109 |
see paper; ..., prominent forehead; brachycephaly; wide anterior fontanel; hypertelorism; no congenital glaucoma; large cornea; prominent eyes; full cheeks; no anteverted nostrils; broad mouth; no broad alveolar ridges; micrognathia; no kyphosis; no prominent coccyx; no bowing long bones; short hands; no flexion deformity fingers; no mitral valve anomaly; ventricular septal defect |
Frank-Ter Haar syndrome |
FTHS |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Johan den Dunnen |
00472306 |
| 0000357110 |
see paper; ..., no prominent forehead; no brachycephaly; wide anterior fontanel; hypertelorism; no congenital glaucoma; large cornea; prominent eyes; full cheeks; anteverted nostrils; broad mouth; broad alveolar ridges; micrognathia; protruding ears; no kyphosis; prominent coccyx; no bowing long bones; no short hands; flexion deformity fingers; no club feet; no mitral valve anomaly; no double right outlet; hypertrophic cardiomyopathy. |
Frank-Ter Haar syndrome |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00472307 |
| 0000357111 |
see paper; ..., no prominent forehead; no brachycephaly; wide anterior fontanel; hypertelorism; no congenital glaucoma; large cornea; prominent eyes; full cheeks; anteverted nostrils; broad mouth; broad alveolar ridges; micrognathia; protruding ears; no kyphosis; prominent coccyx; no bowing long bones; no short hands; flexion deformity fingers; no club feet; no mitral valve anomaly; no double right outlet |
Frank-Ter Haar syndrome |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00472308 |
| 0000357112 |
see paper; ..., motor retardation; prominent forehead; no brachycephaly; hypertelorism; congenital glaucoma; large cornea; prominent eyes; full cheeks; anteverted nostrils; broad mouth; no micrognathia; no protruding ears; no kyphosis; no prominent coccyx; no bowing long bones; no short hands; no flexion deformity fingers; club feet; no mitral valve anomaly; no double right outlet; atrial septal defect; auricular pits |
Frank-Ter Haar syndrome |
− |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00472309 |
| 0000357113 |
see paper; ..., prominent forehead; brachycephaly; wide anterior fontanel; hypertelorism; tetinal detachment, 7y-sudden vision loss; large cornea; prominent eyes; full cheeks; anteverted nostrils; broad mouth; broad alveolar ridges; micrognathia; kyphosis; prominent coccyx; severe genu valgum, dislocated left knee, bilateral hips, both elbows; short hands; no flexion deformity fingers; pes valgus.; cardiomegaly, severe mitral and aortic valve prolapsed; ventricular septal defect |
Frank-Ter Haar syndrome |
FTHS |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Johan den Dunnen |
00472310 |
| 0000357114 |
see paper; ..., motor retardation; prominent forehead; brachycephaly; wide anterior fontanel; hypertelorism; no congenital glaucoma; large cornea; prominent eyes; full cheeks; anteverted nostrils; broad mouth; broad alveolar ridges; micrognathia; protruding ears; kyphosis; prominent coccyx; bowing long bones; short hands; flexion deformity fingers; club feet; no mitral valve anomaly; ventricular septal defect, atrial septal defect, patent ductus arteriosis |
Frank-Ter Haar syndrome |
FTHS |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Johan den Dunnen |
00472311 |
| 0000357115 |
see paper; ..., 8y-deceased; no motor retardation; no acne; coarse face, thick skin; gingival enlargement; prominent forehead; brachycephaly; hypertelorism; no congenital glaucoma; no large cornea; prominent eyes; full cheeks; no anteverted nostrils; broad mouth; broad alveolar ridges; micrognathia; no protruding ears; mitral valve anomaly; no double right outlet; no ventricular septal defect; vertebral anomalies; no prominent coccyx; bowing long bones; short hands; flexion deformity; club feet; osteopenia; genu valgum; radial head dislocation; thoracic wall deformity; thickened interphalangeal joints |
Borrone Dermato-Cardio-Skeletal syndrome |
FTHS |
Familial, autosomal recessive |
8y |
- |
- |
- |
- |
Johan den Dunnen |
00472312 |
| 0000357116 |
see paper; ..., no motor retardation; acne; coarse face, thick skin; no gingival enlargement; prominent forehead; hypertelorism; no prominent eyes; full cheeks; no anteverted nostrils; broad mouth; no micrognathia; no protruding ears; mitral valve anomaly; no double right outlet; no ventricular septal defect; vertebral anomalies; no prominent coccyx; no bowing long bones; short hands; flexion deformity; no club feet; cortical erosions; gynecomastia; thickening interphalangeal joints |
Borrone Dermato-Cardio-Skeletal syndrome |
- |
Unknown |
19y |
- |
- |
- |
- |
Johan den Dunnen |
00472313 |
| 0000357117 |
see paper; ..., no motor retardation; acne; coarse face, thick skin; no gingival enlargement; prominent forehead; hypertelorism; no prominent eyes; full cheeks; no anteverted nostrils; broad mouth; no micrognathia; no protruding ears; mitral valve anomaly; no double right outlet; no ventricular septal defect; no vertebral anomalies; no prominent coccyx; no bowing long bones; short hands; flexion deformity; no club feet; umbilical hernia; thickening interphalangeal joints |
Borrone Dermato-Cardio-Skeletal syndrome |
- |
Unknown |
17y |
- |
- |
- |
- |
Johan den Dunnen |
00472314 |
| 0000357118 |
see paper; ..., no motor retardation; acne; coarse face, thick skin; gingival enlargement; prominent forehead; brachycephaly; hypertelorism; full cheeks; anteverted nostrils; broad mouth; micrognathia; protruding ears; mitral valve anomaly; no double right outlet; no ventricular septal defect; vertebral anomalies; no prominent coccyx; bowing long bones; short hands; flexion deformity; no club feet; cortical erosions; osteoporosis; osteolytic lesions; arthropathy; irregular tongue; inguinal hernia; genu recurvatum |
Borrone Dermato-Cardio-Skeletal syndrome |
FTHS |
Familial, autosomal recessive |
36y |
- |
- |
- |
- |
Johan den Dunnen |
00472315 |
| 0000357119 |
see paper; ..., 24y-deceased; no motor retardation; acne; coarse face, thick skin; gingival enlargement; prominent forehead; hypertelorism; full cheeks; anteverted nostrils; broad mouth; micrognathia; mitral valve anomaly; no double right outlet; no ventricular septal defect; vertebral anomalies; no prominent coccyx; no bowing long bones; short hands; flexion deformity; no club feet; cortical erosions; osteoporosis |
Borrone Dermato-Cardio-Skeletal syndrome |
FTHS |
Familial, autosomal recessive |
23y |
- |
- |
- |
- |
Johan den Dunnen |
00472316 |
|
|
Legend |
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