Deep palmar crease

Symptom Information:

Symptom ID: HPO:0006191
Synonyms:
Deep palmar creases [HPO:0006191]
Deep palmar creases [OMIM:Deep palmar creases]
Deep palmar creases [Orphanet:20280]
Deep palmar creases (1 patient) [OMIM:Deep palmar creases (1 patient)]
Quality:
Cross references:
Orphanet:20280 "Deep palmar creases" [Orphanet:20280]
OMIM: "Deep palmar creases" [OMIM:Deep palmar creases]
OMIM: "Deep palmar creases (1 patient)" [OMIM:Deep palmar creases (1 patient)]
Is a (Direct Parents):
HPO         Abnormality of the palmar creases
Orphanet Abnormality of the hand
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)
                         Deep palmar crease(HPO:0006191)
       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)
                                  Deep palmar crease(HPO:0006191)
MedDRA:
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

19p13.12 microdeletion syndrome (Orphanet:254346)
Acromegaly (Orphanet:963)
Beckwith-Wiedemann syndrome due to NSD1 mutation (Orphanet:238613)
Bohring-Opitz syndrome (Orphanet:97297)
CHARGE syndrome (Orphanet:138)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Costello syndrome (Orphanet:3071)
Miller-Dieker syndrome (Orphanet:531)
Mosaic trisomy 8 (Orphanet:96061)
Mosaic trisomy 9 (Orphanet:99776)
Mowat-Wilson syndrome (Orphanet:2152)
PLANTAR LIPOMATOSIS, UNUSUAL FACIES, AND DEVELOPMENTAL DELAY (OMIM:602342)
TARP syndrome (Orphanet:2886)
Tessier number 4 facial cleft (Orphanet:141258)
Trisomy 8q (Orphanet:1752)
Wrinkly skin syndrome (Orphanet:2834)