Absent palmar crease

Symptom Information:

Symptom ID: HPO:0010489
Synonyms:
Absence of the palmar creases [HPO:0010489]
Aplasia of the palmar creases [HPO:0010489]
Absence of palmar creases [Orphanet:20260]
Quality:
Cross references:
Orphanet:20260 "Absence of palmar creases" [Orphanet:20260]
Is a (Direct Parents):
Orphanet Abnormality of the hand
HPO         Aplasia/Hypoplasia of the palmar creases
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)
                   Abnormal palmar dermatoglyphics(HPO:0001018)
                      Abnormality of the palmar creases(HPO:0010490)
                         Aplasia/Hypoplasia of the palmar creases(HPO:0010488)
                            Absent palmar crease(HPO:0010489)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the upper limb(HPO:0002817)
                      Abnormality of the hand(HPO:0001155)
                         Abnormality of the palm(HPO:0100871)
                            Abnormal palmar dermatoglyphics(HPO:0001018)
                               Abnormality of the palmar creases(HPO:0010490)
                                  Aplasia/Hypoplasia of the palmar creases(HPO:0010488)
                                     Absent palmar crease(HPO:0010489)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

8q21.11 microdeletion syndrome (Orphanet:284160)
Arthrogryposis with oculomotor limitation and electroretinal anomalies (Orphanet:1154)
Ehlers-Danlos syndrome, spondylocheirodysplastic type (Orphanet:157965)
Fetal akinesia deformation sequence (Orphanet:994)
Freeman-Sheldon syndrome (Orphanet:2053)