The Cornelia de Lange Syndrome Foundation
Historical collection: May 2019 · Rating details mostly from 2017. Source & context
What this organization describes
Reaching out, providing help, giving hope
Mission and tagline reproduced from the source record.
Three perspectives. One record.
out of 100
out of 100
out of 100
These are the dataset’s historical numeric fields, not a current rating or a new DonorAPI.com assessment. Read the score context ↗
Revenue, expenses, and composition
Program expenses
$825,300.82 recorded amountFundraising expenses
$63,925.04 recorded amountAdministrative expenses
$62,970.93 recorded amount- Fundraising efficiency
- $0.08 spent per $1 raised in donations, as defined in the source.
Expense shares are displayed as percentages. Component amounts in this collection match total expenses multiplied by the source ratios; rounding can leave a small difference from the total. The source does not supply a row-specific fiscal year. Field definitions ↗
The leadership information supplied
- Recorded leader
- Morrisette Royster
- Recorded compensation
- $99,000.00
- Recorded compensation percentage
- 10.37%
These fields do not establish the current officeholder or current compensation. The metadata does not specify the denominator of the leader compensation percentage. Read with context ↗
Inspect all 23 original source fields
Exact source strings are retained below, including numeric precision. A blank value is marked as not reported; zero remains zero.
| Source field | Original source value |
|---|---|
ascoreAccountability & transparency score | 96.0 |
categoryCategory | Health |
descriptionMission & description | Founded in 1981, The Cornelia de Lange Syndrome (CdLS) Foundation is a family support organization which exists to ensure early and accurate diagnosis of CdLS, promote research into the causes and manifestations of the syndrome, and help people with a diagnosis of CdLS, and others with similar characteristics, make informed decisions throughout their lifetime. The Foundation provides a host of services that attract, educate, and unite families touched by this rare birth disorder which causes individuals to develop at a slower rate, both physically and mentally. CdLS is a congenital syndrome, and individuals affected have common characteristics such as: low birth weight, slow growth and small stature, small head size, and limb differences. |
einEIN | 06-1057497 |
tot_expTotal expenses | 954105.0 |
admin_exp_pAdministrative expense fraction | 0.066 |
fund_effFundraising efficiency ($ per $1 raised) | 0.08 |
fund_exp_pFundraising expense fraction | 0.067 |
program_exp_pProgram expense fraction | 0.865 |
fscoreFinancial score | 90.0 |
leaderRecorded leader | Morrisette Royster |
leader_compRecorded leader compensation | 99000.0 |
leader_comp_pRecorded leader compensation fraction | 0.10369999999999999 |
mottoTagline | Reaching out, providing help, giving hope |
nameCharity name | The Cornelia de Lange Syndrome Foundation |
tot_revTotal revenue | 962849.0 |
scoreOverall score | 92.38 |
stateState code | CT |
subcategorySubcategory | Diseases, Disorders, and Disciplines |
sizeSource size label | small |
program_expProgram expenses | 825300.825 |
fund_expFundraising expenses | 63925.035 |
admin_expAdministrative expenses | 62970.93 |
Source: Charity Navigator Scores Expenses Dataset, version 1, attributed to katyjqian on Kaggle. Collection: May 2019; rating details mostly from 2017. Read attribution, scope, and reuse notes.