Single transverse palmar crease
Symptom Information:
Symptom ID: | HPO:0000954 | ||||||||||||||||||||||||||
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) 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) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Skin and subcutaneous tissue disorders NEC(MedDRA:10040790) Skin and subcutaneous conditions NEC(MedDRA:10042356) Single transverse palmar crease(HPO:0000954) |
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Database Frequency: | 162 / 7739 | ||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
14q22q23 microdeletion syndrome | (Orphanet:264200) |
15q24 microdeletion syndrome | (Orphanet:94065) |
16p11.2p12.2 microdeletion syndrome | (Orphanet:261211) |
17q23.1q23.2 microdeletion syndrome | (Orphanet:261279) |
2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
2q37 microdeletion syndrome | (Orphanet:1001) |
3-methylglutaconic aciduria type 4 | (Orphanet:67048) |
AARSKOG SYNDROME, AUTOSOMAL DOMINANT | (OMIM:100050) |
AARSKOG-SCOTT SYNDROME | (OMIM:305400) |
ADAMS-OLIVER SYNDROME 2 | (OMIM:614219) |
ARTHROGRYPOSIS, DISTAL, TYPE 1A | (OMIM:108120) |
ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 3 | (OMIM:170995) |
Aarskog-Scott syndrome | (Orphanet:915) |
Absence of fingerprints - congenital milia | (Orphanet:1658) |
Acro-oto-ocular syndrome | (Orphanet:2980) |
Acrofacial dysostosis, Catania type | (Orphanet:1786) |
Acrofacial dysostosis, Rodriguez type | (Orphanet:1788) |
Acromesomelic dysplasia, Hunter-Thomson type | (Orphanet:968) |
Allan-Herndon-Dudley syndrome | (Orphanet:59) |
Anonychia - microcephaly | (Orphanet:1094) |
Antenatal multiminicore disease with arthrogryposis multiplex congenita | (Orphanet:178148) |
Aplasia cutis congenita - intestinal lymphangiectasia | (Orphanet:1116) |
Ataxia - photosensitivity - short stature | (Orphanet:1184) |
Autosomal recessive Robinow syndrome | (Orphanet:1507) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY | (OMIM:210550) |
BRACHYMESOMELIA-RENAL SYNDROME | (OMIM:113470) |
Blepharophimosis-intellectual deficit syndrome, SBBYS type | (Orphanet:3047) |
Branchio-oculo-facial syndrome | (Orphanet:1297) |
Böök syndrome | (Orphanet:1262) |
C syndrome | (Orphanet:1308) |
CATEL-MANZKE SYNDROME | (OMIM:616145) |
CHROMOSOME 6q11-q14 DELETION SYNDROMECHROMOSOME 6q13-q14 DELETION SYNDROME, INCLUDED | (OMIM:613544) |
CHST3-related skeletal dysplasia | (Orphanet:263463) |
COFFIN-SIRIS SYNDROME | (OMIM:135900) |
CORNELIA DE LANGE SYNDROME 1 | (OMIM:122470) |
Camptodactyly syndrome, Guadalajara type 2 | (Orphanet:1326) |
Cataract - deafness - hypogonadism | (Orphanet:1383) |
Catel-Manzke syndrome | (Orphanet:1388) |
Cleidorhizomelic syndrome | (Orphanet:1453) |
Coffin-Lowry syndrome | (Orphanet:192) |
Coffin-Siris syndrome | (Orphanet:1465) |
Cohen syndrome | (Orphanet:193) |
Conductive deafness - ptosis - skeletal anomalies | (Orphanet:3236) |
Congenital bile acid synthesis defect type 4 | (Orphanet:79095) |
Cornelia de Lange syndrome | (Orphanet:199) |
Cranioectodermal dysplasia | (Orphanet:1515) |
Cranioectodermal dysplasia 1 | (OMIM:218330) |
Craniosynostosis - fibular aplasia | (Orphanet:1533) |
Cryptorchidism - arachnodactyly - intellectual deficit | (Orphanet:1548) |
DESBUQUOIS DYSPLASIA 2 | (OMIM:615777) |
DPAGT1-CDG | (Orphanet:86309) |
Digitotalar dysmorphism | (Orphanet:1146) |
Distal monosomy 10p | (Orphanet:1580) |
Distal monosomy 17q | (Orphanet:1597) |
Distal monosomy 7q36 | (Orphanet:1636) |
Distal trisomy 18q | (Orphanet:1716) |
Down syndrome | (Orphanet:870) |
EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 1 | (OMIM:130070) |
Ehlers-Danlos syndrome, progeroid type | (Orphanet:75496) |
Extrasystoles - short stature - hyperpigmentation - microcephaly | (Orphanet:1964) |
Fetal trimethadione syndrome | (Orphanet:1913) |
Fibular aplasia - complex brachydactyly | (Orphanet:2639) |
Filippi syndrome | (Orphanet:3255) |
Frontonasal dysplasia | (Orphanet:250) |
Fryns syndrome | (Orphanet:2059) |
Fuhrmann syndrome | (Orphanet:2854) |
Gonadal dysgenesis, XY type - associated anomalies | (Orphanet:1770) |
Gordon syndrome | (Orphanet:376) |
Intellectual deficit - athetosis - microphthalmia | (Orphanet:1236) |
Intellectual deficit - hypotonia - skin hyperpigmentation | (Orphanet:3050) |
Intellectual deficit - spasticity - ectrodactyly | (Orphanet:1891) |
Intellectual deficit, X-linked - cubitus valgus - dysmorphism | (Orphanet:85280) |
Intellectual deficit, X-linked - seizures - psoriasis | (Orphanet:3052) |
Intellectual deficit, X-linked, Wittwer type | (Orphanet:85291) |
Isolated plagiocephaly | (Orphanet:35098) |
Johanson-Blizzard syndrome | (Orphanet:2315) |
KBG syndrome | (Orphanet:2332) |
Kapur-Toriello syndrome | (Orphanet:2328) |
Kleefstra syndrome | (Orphanet:261494) |
Langer-Giedion syndrome | (Orphanet:502) |
Laurence-Moon syndrome | (Orphanet:2377) |
Lethal Larsen-like syndrome | (Orphanet:2371) |
Lethal faciocardiomelic dysplasia | (Orphanet:1972) |
Lichstenstein syndrome | (Orphanet:2390) |
Low birth weight - dwarfism - dysgammaglobulinemia | (Orphanet:2621) |
Lung agenesis - heart defect - thumb anomalies | (Orphanet:1120) |
MACS syndrome | (Orphanet:217335) |
MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE | (OMIM:300861) |
MULTIPLE SYNOSTOSES SYNDROME 1 | (OMIM:186500) |
Marden-Walker syndrome | (Orphanet:2461) |
Maternal hyperthermia induced birth defects | (Orphanet:2216) |
McDonough syndrome | (Orphanet:2471) |
Melhem-Fahl syndrome | (Orphanet:2482) |
Mesoaxial synostotic syndactyly with phalangeal reduction | (Orphanet:157801) |
Mesomelic dwarfism, Nievergelt type | (Orphanet:2633) |
Microbrachycephaly - ptosis - cleft lip | (Orphanet:2511) |
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 | (Orphanet:2636) |
Microcephaly - cardiac defect - lung malsegmentation | (Orphanet:2516) |
Microcephaly - intellectual deficit - phalangeal and neurological anomalies | (Orphanet:137658) |
Microlissencephaly - micromelia | (Orphanet:50810) |
Microphthalmia with brain and digit anomalies | (Orphanet:139471) |
Microphthalmia with limb anomalies | (Orphanet:1106) |
Miller-Dieker syndrome | (Orphanet:531) |
Monosomy 5p | (Orphanet:281) |
Monosomy 9p | (Orphanet:261112) |
Mosaic trisomy 14 | (Orphanet:1703) |
Multiple synostoses syndrome | (Orphanet:3237) |
Neonatal adrenoleukodystrophy | (Orphanet:44) |
Non-distal monosomy 10q | (Orphanet:1581) |
OPITZ-KAVEGGIA SYNDROME | (OMIM:305450) |
Oculocerebrofacial syndrome, Kaufman type | (Orphanet:2707) |
Odonto-tricho-ungual-digito-palmar syndrome | (Orphanet:69082) |
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) | (OMIM:214100) |
PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER) | (OMIM:214110) |
PEROXISOME BIOGENESIS DISORDER 3B | (OMIM:266510) |
PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER) | (OMIM:614866) |
Penoscrotal transposition | (Orphanet:2842) |
Perlman syndrome | (Orphanet:2849) |
Peters-plus syndrome | (Orphanet:709) |
Pitt-Hopkins syndrome | (Orphanet:2896) |
Postaxial tetramelic oligodactyly | (Orphanet:2730) |
Potocki-Shaffer syndrome | (Orphanet:52022) |
Prader-Willi syndrome | (Orphanet:739) |
Prolidase deficiency | (Orphanet:742) |
Prominent glabella - microcephaly - hypogenitalism | (Orphanet:2083) |
Rasmussen-Johnsen-Thomsen syndrome | (Orphanet:3023) |
Recombinant 8 syndrome | (Orphanet:96167) |
Renal tubular dysgenesis | (Orphanet:3033) |
Roberts syndrome | (Orphanet:3103) |
Roifman syndrome | (Orphanet:353298) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |
Rudiger syndrome | (Orphanet:3118) |
SECKEL SYNDROME 1 | (OMIM:210600) |
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY | (OMIM:614800) |
SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION,LETHAL | (OMIM:602613) |
Saethre-Chotzen syndrome | (Orphanet:794) |
Schilbach-Rott syndrome | (Orphanet:2353) |
Schinzel-Giedion syndrome | (Orphanet:798) |
Seckel syndrome | (Orphanet:808) |
Sheldon-Hall syndrome | (Orphanet:1147) |
Short rib-polydactyly syndrome | (Orphanet:1505) |
Short rib-polydactyly syndrome, Beemer-Langer type | (Orphanet:93268) |
Short stature - heart defect - craniofacial anomalies | (Orphanet:1088) |
Sillence syndrome | (Orphanet:3168) |
Simpson-Golabi-Behmel syndrome type 2 | (Orphanet:79022) |
Stüve-Wiedemann syndrome | (Orphanet:3206) |
Subaortic stenosis - short stature | (Orphanet:3191) |
TARP syndrome | (Orphanet:2886) |
Teebi-Shaltout syndrome | (Orphanet:3291) |
Tetrasomy 12p | (Orphanet:884) |
Trisomy 13 | (Orphanet:3378) |
Trisomy 18 | (Orphanet:3380) |
Trisomy 9p | (Orphanet:236) |
WT limb-blood syndrome | (Orphanet:3466) |
Warsaw breakage syndrome | (Orphanet:280558) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |
X-linked distal arthrogryposis multiplex congenita | (Orphanet:1145) |
Yunis-Varon syndrome | (Orphanet:3472) |
Zellweger syndrome | (Orphanet:912) |
Zellweger-like syndrome without peroxisomal anomalies | (Orphanet:50812) |
Zlotogora-Ogur syndrome | (Orphanet:3253) |