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
|
| 0000175663 |
split-hand/foot malformation |
SHFM-6 |
split-hand/foot malformation |
Familial, autosomal recessive |
- |
- |
- |
- |
Johan den Dunnen |
00235401 |
| 0000175664 |
split-hand/foot malformation, femoral bifurcation (Gollop-Wolfgang complex) |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/L; ectrodactyly feet (HP:0001839) R/L; long bone deficiency (HP:0011314) R/L tibia; long bone deficiency (HP:0011314) R/- femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235402 |
| 0000175668 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/L; ectrodactyly feet (HP:0001839) -/L; no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235406 |
| 0000175669 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/-; no ectrodactyly feet (-HP:0001839); no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235407 |
| 0000175673 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/-; ectrodactyly feet (HP:0001839) -/L; no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235411 |
| 0000175674 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/-; no ectrodactyly feet (-HP:0001839); no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235412 |
| 0000175675 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/L; no ectrodactyly feet (-HP:0001839); no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235413 |
| 0000175676 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/L; no ectrodactyly feet (-HP:0001839); no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235414 |
| 0000175677 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/-; ectrodactyly feet (HP:0001839) R/-; no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235415 |
| 0000175678 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/-; ectrodactyly feet (HP:0001839) R/-; no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235416 |
| 0000175679 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/L; no ectrodactyly feet (-HP:0001839); no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235417 |
| 0000175680 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/L; no ectrodactyly feet (-HP:0001839); no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235418 |
| 0000175681 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/L; no ectrodactyly feet (-HP:0001839); no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235419 |
| 0000175682 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/-; no ectrodactyly feet (-HP:0001839); no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235420 |
| 0000175683 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) -/L; no ectrodactyly feet (-HP:0001839); no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235421 |
| 0000175684 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/-; no ectrodactyly feet (-HP:0001839); no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235422 |
| 0000175685 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/-; no ectrodactyly feet (-HP:0001839); no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235423 |
| 0000175686 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) -/L; no ectrodactyly feet (-HP:0001839); no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235424 |
| 0000175687 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/L; no ectrodactyly feet (-HP:0001839); no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235425 |
| 0000175688 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) -/L; no ectrodactyly feet (-HP:0001839); no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235426 |
| 0000175689 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/-; no ectrodactyly feet (-HP:0001839); no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235427 |
| 0000175690 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/-; no ectrodactyly feet (-HP:0001839); no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235428 |
| 0000175691 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/-; no ectrodactyly feet (-HP:0001839); no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235429 |
| 0000175692 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/L; ectrodactyly feet (HP:0001839) R/L; no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235430 |
| 0000175693 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/L; no ectrodactyly feet (-HP:0001839); no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235431 |
| 0000175694 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/L; ectrodactyly feet (HP:0001839) R/-; no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235432 |
| 0000175695 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/L; no ectrodactyly feet (-HP:0001839); no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235433 |
| 0000175696 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/L; no ectrodactyly feet (-HP:0001839); no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235434 |
| 0000175697 |
split-hand/foot malformation, femoral bifurcation (Gollop-Wolfgang complex) |
SHFLD-3 |
ectrodactyly hand (HP:0001171) -/L; ectrodactyly feet (HP:0001839) R/-; long bone deficiency (HP:0011314) R/L tibia; long bone deficiency (HP:0011314) R/- femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235435 |
| 0000175702 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/L; no ectrodactyly feet (-HP:0001839); no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235440 |
| 0000175704 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) R/L; ectrodactyly feet (HP:0001839) R/L; no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235442 |
| 0000175705 |
split-hand/foot malformation |
SHFLD-3 |
ectrodactyly hand (HP:0001171) -/L; ectrodactyly feet (HP:0001839) -/L; no long bone deficiency (-HP:0011314) tibia; no long bone deficiency (-HP:0011314) femur |
Familial, autosomal dominant |
- |
- |
- |
- |
Johan den Dunnen |
00235443 |
| 0000300289 |
split-hand/foot malformation |
- |
see paper; ..., split hand/foot malformation, long bone deficiency |
Unknown |
- |
- |
- |
- |
Johan den Dunnen |
00408160 |