Absent digit

Polydactyly or polydactylism (from Greek πολύς (polys) 'many', and δάκτυλος (daktylos) 'finger'), also known as hyperdactyly, is an anomaly in humans and animals resulting in supernumerary fingers and/or toes. Polydactyly is the opposite of oligodactyly (fewer fingers or toes). [Source: Wikipedia ]

Synonyms
Digital absence
Subtypes
Adactyly
Aphalangy
Monodactyly
Oligodactyly
May Be Caused by
Acheiropodia
Acrofacial dysostosis
Acrorenal syndrome
Amniotic band syndrome
Anonychia-ectrodactyly syndrome
Aplasia cutis congenita
Atelosteogenesis
Baller-Gerold syndrome
Brachmann-de Lange syndrome
CCGE syndrome
Cenani-Lenz syndactyly syndrome
Charlie M syndrome
CHILD syndrome
Chorionic villus sampling-transverse limb deficiency
Chromosome 2q24-q31 deletion
Cocaine abuse
DOOR syndrome
EEC syndrome
Eronen syndrome
Femur-fibula-ulna syndrome
Fetal hydantoin syndrome
Fetal phenytoin toxicity
Fetal pyrimethamine syndrome
Fryns syndrome
Fuhrmann syndrome
Glossopalatine ankylosis syndrome
Goltz syndrome
Grebe chondrodysplasia
Hand-foot-genital syndrome
Hanhart syndrome
Holt-Oram syndrome
Humeroradioulnar synostosis and oligoectrosyndactyly
Hypoglossia-hypodactyly
Marles-Chudley syndrome
Melnick-Needles osteodysplasty
Mesomelic dysplasia Werner type
Möbius syndrome
Oculo-dento-osseous dysplasia
Ophthalmo-acromelic syndrome
Opitz trigonocephaly syndrome
Orofaciodigital syndrome type 1
Oromandibular-limb hypogenesis syndrome
PIV syndrome
Poland syndrome
Postaxial acrofacial dysostosis syndrome Miller type
Pterygium syndrome
Roberts syndrome
Splenogonadal fusion-limb deformity syndrome
Split-hand split-foot deformity
Symbrachydactyly-oligodactyly
Tetramelic postaxial oligodactyly
Thalidomide embryopathy
Trisomy 13
Trisomy 18
Trisomy 21
Turner syndrome
Tylosis
Ulnar aplasia with foot ectrodactyly
Ulnar-mammary syndrome
Unilateral terminal transverse hand defect
Waardenburg anophthalmia syndrome
Weyers oligodactyly syndrome
Yunis-Varon syndrome
Zimmermann-Laband syndrome
Digital absence
Acheiropodia
Acrofacial dysostosis
Acrorenal syndrome
Amniotic band syndrome
Anonychia-ectrodactyly syndrome
Aplasia cutis congenita
Atelosteogenesis
Baller-Gerold syndrome
Brachmann-de Lange syndrome
CCGE syndrome
Cenani-Lenz syndactyly syndrome
Charlie M syndrome
CHILD syndrome
Chorionic villus sampling-transverse limb deficiency
Chromosome 2q24-q31 deletion
Cocaine abuse
DOOR syndrome
EEC syndrome
Eronen syndrome
Femur-fibula-ulna syndrome
Fetal hydantoin syndrome
Fetal phenytoin toxicity
Fetal pyrimethamine syndrome
Fryns syndrome
Fuhrmann syndrome
Glossopalatine ankylosis syndrome
Goltz syndrome
Grebe chondrodysplasia
Hand-foot-genital syndrome
Hanhart syndrome
Holt-Oram syndrome
Humeroradioulnar synostosis and oligoectrosyndactyly
Hypoglossia-hypodactyly
Marles-Chudley syndrome
Melnick-Needles osteodysplasty
Mesomelic dysplasia Werner type
Möbius syndrome
Oculo-dento-osseous dysplasia
Ophthalmo-acromelic syndrome
Opitz trigonocephaly syndrome
Orofaciodigital syndrome type 1
Oromandibular-limb hypogenesis syndrome
PIV syndrome
Poland syndrome
Postaxial acrofacial dysostosis syndrome Miller type
Pterygium syndrome
Roberts syndrome
Splenogonadal fusion-limb deformity syndrome
Split-hand split-foot deformity
Symbrachydactyly-oligodactyly
Tetramelic postaxial oligodactyly
Thalidomide embryopathy
Trisomy 13
Trisomy 18
Trisomy 21
Turner syndrome
Tylosis
Ulnar aplasia with foot ectrodactyly
Ulnar-mammary syndrome
Unilateral terminal transverse hand defect
Waardenburg anophthalmia syndrome
Weyers oligodactyly syndrome
Yunis-Varon syndrome
Zimmermann-Laband syndrome