| manager |
|
| language |
- |
| license |
- |
| created at |
2024-09-19 07:43:07 UTC |
| updated at |
2024-09-23 18:19:38 UTC |
|
MedGen CUI
Namespace: https://www.ncbi.nlm.nih.gov/medgen/
|
622,528 entries
|
There is 0 pattern entry.
|
Syndrome, Pfeiffer
|
C0220658 |
|
|
Syndromes, Noack
|
C0220658 |
|
|
craniofacial-skeletal-Dermatologic dysplasia
|
C0220658 |
|
|
ACROCEPHALOSYNDACTYLY, TYPE V
|
C0220658 |
|
|
Acrocephalosyndactylies, Type V
|
C0220658 |
|
|
Acrocephalosyndactyly type V
|
C0220658 |
|
|
Acrocephalosyndactyly, Type V
|
C0220658 |
|
|
acrocephalosyndactylia type V
|
C0220658 |
|
|
acrocephalosyndactyly type V
|
C0220658 |
|
|
Pfeiffer type acrocephalosyndactyly
|
C0220658 |
|
|
Acrocephalosyndactyly type 5
|
C0220658 |
|
|
Acrocephalosyndactyly, type 5
|
C0220658 |
|
|
acrocephalosyndactyly type 5
|
C0220658 |
|
|
acrocephalosyndactyly, type 5
|
C0220658 |
|
|
Type V Acrocephalosyndactylies
|
C0220658 |
|
