Clinodactyly of fifth finger

Clinodactyly is a medical term describing the curvature of a digit (a finger or toe) in the plane of the palm, most commonly the fifth finger (the "pinkie finger") towards the adjacent fourth finger (the "ring finger"). It is a fairly common isolated anomaly which often goes unnoticed, but also occurs in combination with other abnormalities in certain genetic syndromes. [Source: Wikipedia ]

Synonyms
Incurving of fifth digit with hypoplastic short middle phalanx
May Be Caused by
Aarskog syndrome
Acrocephalopolysyndactyly
Acrocephalosyndactyly Saethre-Chotzen type
Aminopterin fetopathy
Arthritis
Bardet-Biedl syndrome
Bloom syndrome
Brachmann-de Lange syndrome
Campomelic dysplasia
Chromosome 4p- syndrome
Chromosome 5:del(5p) syndrome
Coffin-Siris syndrome
Cohen syndrome
Contracture
DOOR syndrome
Dubowitz syndrome
EEC syndrome
Ehlers-Danlos syndrome
Familial brachydactyly A1
Familial brachydactyly A2
Familial brachydactyly A3
Familial brachydactyly A4
Familial brachydactyly C
Fanconi anemia
Fetal alcohol syndrome
Fibrochondrogenesis
Fibrodysplasia ossificans progressiva
Goltz syndrome
Goodman syndrome
Hand-foot-genital syndrome
Holt-Oram syndrome
Hypomelanosis of Ito
Isolated clinodactyly of fifth finger
Klinefelter syndrome
Lacrimo-auriculo-dento-digital syndrome
Laurence-Moon syndrome
Lenz microphthalmia syndrome
Marfan syndrome
Meckel syndrome
Mesomelic dysplasia Nievergelt type
Mitral valve prolapse syndrome
Nail-patella syndrome
Noonan syndrome
Normal variant
Oculo-dento-osseous dysplasia
Orofaciodigital syndrome type 1
Orofaciodigital syndrome type 2
Poland syndrome
Popliteal pterygium syndrome
Prader-Willi syndrome
Rieger syndrome
Roberts syndrome
Robinow syndrome
Rubinstein-Taybi syndrome
Seckel syndrome
Shwachman–Diamond syndrome
Silver-Russell syndrome
Symphalangism-surdity syndrome
TAR syndrome
Trauma
Treacher Collins syndrome
Trichorhinophalangeal dysplasia type 1
Trichorhinophalangeal dysplasia type 2
Trichorhinophalangeal dysplasia type 3
Triploidy
Trisomy 13
Trisomy 18
Trisomy 21
Trisomy 8
Trisomy 9p
Weill-Marchesani syndrome
Williams syndrome
XXXX syndrome
XXXXX syndrome
XXXXY syndrome
XXXY syndrome
Zellweger syndrome
Incurving of fifth digit with hypoplastic short middle phalanx
Aarskog syndrome
Acrocephalopolysyndactyly
Acrocephalosyndactyly Saethre-Chotzen type
Aminopterin fetopathy
Arthritis
Bardet-Biedl syndrome
Bloom syndrome
Brachmann-de Lange syndrome
Campomelic dysplasia
Chromosome 4p- syndrome
Chromosome 5:del(5p) syndrome
Coffin-Siris syndrome
Cohen syndrome
Contracture
DOOR syndrome
Dubowitz syndrome
EEC syndrome
Ehlers-Danlos syndrome
Familial brachydactyly A1
Familial brachydactyly A2
Familial brachydactyly A3
Familial brachydactyly A4
Familial brachydactyly C
Fanconi anemia
Fetal alcohol syndrome
Fibrochondrogenesis
Fibrodysplasia ossificans progressiva
Goltz syndrome
Goodman syndrome
Hand-foot-genital syndrome
Holt-Oram syndrome
Hypomelanosis of Ito
Isolated clinodactyly of fifth finger
Klinefelter syndrome
Lacrimo-auriculo-dento-digital syndrome
Laurence-Moon syndrome
Lenz microphthalmia syndrome
Marfan syndrome
Meckel syndrome
Mesomelic dysplasia Nievergelt type
Mitral valve prolapse syndrome
Nail-patella syndrome
Noonan syndrome
Normal variant
Oculo-dento-osseous dysplasia
Orofaciodigital syndrome type 1
Orofaciodigital syndrome type 2
Poland syndrome
Popliteal pterygium syndrome
Prader-Willi syndrome
Rieger syndrome
Roberts syndrome
Robinow syndrome
Rubinstein-Taybi syndrome
Seckel syndrome
Shwachman–Diamond syndrome
Silver-Russell syndrome
Symphalangism-surdity syndrome
TAR syndrome
Trauma
Treacher Collins syndrome
Trichorhinophalangeal dysplasia type 1
Trichorhinophalangeal dysplasia type 2
Trichorhinophalangeal dysplasia type 3
Triploidy
Trisomy 13
Trisomy 18
Trisomy 21
Trisomy 8
Trisomy 9p
Weill-Marchesani syndrome
Williams syndrome
XXXX syndrome
XXXXX syndrome
XXXXY syndrome
XXXY syndrome
Zellweger syndrome