Narrow palpebral fissure
Symptom Information:
Symptom ID: | HPO:0045025 | |
Synonyms: |
|
|
Quality: | ||
Cross references: |
|
|
Is a (Direct Parents): |
|
|
Is a (Whole tree): |
HPO:
MedDRA: |
|
Database Frequency: | 8 / 7739 | |
Resource: | HPO |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
ADAMS-OLIVER SYNDROME 2 | (OMIM:614219) |
CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME | (OMIM:613603) |
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB | (OMIM:614437) |
Dandy-Walker malformation - postaxial polydactyly | (Orphanet:1566) |
Gorlin-Chaudhry-Moss syndrome | (Orphanet:2095) |
Monosomy 9p | (Orphanet:261112) |
Pseudoaminopterin syndrome | (Orphanet:221120) |