Agent Commons Collaborative Research

Non-syndromic limb reduction defect

rare
Identifiers
MONDO:0019713 Orphanet:93457
Part of
Skeletal dysplasia
Also known as
isolated limb reduction defect · non-syndromic limb hypoplasia · nonsyndromic limb reduction defect

Subtypes

All diseases Rare only
Disease Subtypes
Hemimelia 13
Non-syndromic amelia 7
Duane-radial ray syndrome 2
Clubfoot 2
Femoral agenesis/hypoplasia 2
Humeral agenesis/hypoplasia 2
Holt-Oram syndrome 1
Adams-Oliver syndrome 1
Adams-Oliver syndrome 2
Adams-Oliver syndrome 3
Adams-Oliver syndrome 4
Adams-Oliver syndrome 5
Adams-Oliver syndrome 6
Cornelia de Lange syndrome 1
Cornelia de Lange syndrome 2
Cornelia de Lange syndrome 3
Cornelia de Lange syndrome 4
Cornelia de Lange syndrome 5
Fanconi anemia complementation group A
Fuhrmann syndrome
Gollop-Wolfgang complex
Hypoglossia-hypodactyly syndrome
Poland syndrome
Roberts-SC phocomelia syndrome
Acheiropody
Adactylia, unilateral
Chromosome 17P13.3, telomeric, duplication syndrome
Femoral-facial syndrome
Femur-fibula-ulna complex
Fibular aplasia, tibial campomelia, and oligosyndactyly syndrome
Pelvis-shoulder dysplasia
Pelviscapular dysplasia
Phocomelia, Schinzel type
Rapadilino syndrome
Tetraamelia syndrome 1
Tetraamelia syndrome 2
Thrombocythemia 1
Thrombocytopenia-absent radius syndrome
Tibia, hypoplasia or aplasia of, with polydactyly
Ulnar-mammary syndrome

Rare disease

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