Bilateral single transverse palmar creases

Symptom Information:

Symptom ID: HPO:0007598
Synonyms:
Single transverse palmar crease [Orphanet:20200]
Single transverse palmar crease (finding) [Orphanet:20200]
Bilateral single transverse palmar creases [OMIM:Bilateral single transverse palmar creases]
Simian crease/transverse/unique palmar crease [Orphanet:20200]
Simian crease [Orphanet:20200]
Abnormal palmar/plantar creases [MedDRA:10000162]
Abnormal single palmar crease [MedDRA:10000162]
Simian crease [MedDRA:10000162]
Simian crease (in some patients) [OMIM:Simian crease (in some patients)]
Single transverse palmar crease (in some patients) [OMIM:Single transverse palmar crease (in some patients)]
Quality:
Cross references:
HPO:0000954 "Single transverse palmar crease" [Orphanet:20200]
Orphanet:20200 "Simian crease/transverse/unique palmar crease" [Orphanet:20200]
OMIM: "Bilateral single transverse palmar creases" [OMIM:Bilateral single transverse palmar creases]
OMIM: "Simian crease (in some patients)" [OMIM:Simian crease (in some patients)]
OMIM: "Single transverse palmar crease (in some patients)" [OMIM:Single transverse palmar crease (in some patients)]
UMLS:C0424731 "Single transverse palmar crease" [Orphanet:20200]
Is a (Direct Parents):
MedDRA Skin and subcutaneous conditions NEC
Orphanet Abnormality of the hand
HPO         Single transverse palmar crease
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)
                         Single transverse palmar crease(HPO:0000954)
                            Bilateral single transverse palmar creases(HPO:0007598)
       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)
                                  Single transverse palmar crease(HPO:0000954)
                                     Bilateral single transverse palmar creases(HPO:0007598)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Skin and subcutaneous tissue disorders NEC(MedDRA:10040790)
       Skin and subcutaneous conditions NEC(MedDRA:10042356)
          Bilateral single transverse palmar creases(HPO:0007598)
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

3-methylglutaconic aciduria type 4 (Orphanet:67048)
Absence of fingerprints - congenital milia (Orphanet:1658)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
CHST3-related skeletal dysplasia (Orphanet:263463)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Catel-Manzke syndrome (Orphanet:1388)
EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICALTALUS (OMIM:133705)
Hennekam syndrome (Orphanet:2136)
Kapur-Toriello syndrome (Orphanet:2328)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY (OMIM:614800)
Sillence syndrome (Orphanet:3168)
Zellweger-like syndrome without peroxisomal anomalies (Orphanet:50812)