Bilateral single transverse palmar creases
Symptom Information:
Symptom ID: | HPO:0007598 | ||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) 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) 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) 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) |
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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) |