Adermatoglyphia

Symptom Information:

Symptom ID: HPO:0007455
Synonyms:
Adermatoglyphia [OMIM:Adermatoglyphia]
Quality:
Cross references:
OMIM: "Adermatoglyphia" [OMIM:Adermatoglyphia]
UMLS:C1852150 "Adermatoglyphia" [HPO:0007455]
Is a (Direct Parents):
HPO         Abnormal dermatoglyphics
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Regional abnormality of skin(HPO:0011356)
                Abnormal dermatoglyphics(HPO:0007477)
                   Adermatoglyphia(HPO:0007455)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

ADULT syndrome (Orphanet:978)
Absence of fingerprints - congenital milia (Orphanet:1658)
Dermatopathia pigmentosa reticularis (Orphanet:86920)
Isolated adermatoglyphia (Orphanet:289465)