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File:Autosomal recessive - en.svg
From WikiMD's Food, Medicine & Wellness Encyclopedia
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Original file (SVG file, nominally 738 × 1,283 pixels, file size: 29 KB)
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Date/Time | Thumbnail | Dimensions | User | Comment | |
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current | 22:38, 5 October 2023 | 738 × 1,283 (29 KB) | Andreyyshore | attempting to fix font size and spacing for newly-added languages |
File usage
The following file is a duplicate of this file (more details):
- File:Autosomal recessive - en.svg from Wikimedia Commons
The following 92 pages use this file:
- 2-Methylbutyryl-CoA dehydrogenase deficiency
- AREDYLD syndrome
- Adenosine deaminase deficiency
- Alpha-aminoadipic and alpha-ketoadipic aciduria
- Aromatase deficiency
- Aspartylglucosaminuria
- Autosomal recessive bestrophinopathy
- Autosomal recessive isolated ectopia lentis
- Bangstad syndrome
- Buphthalmos
- Buttien-Fryns syndrome
- CD55 deficiency
- Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- Cerebral palsy
- Chondrodysplasia Blomstrand
- Chronic enteropathy associated with SLCO2A1 gene
- Corneal-cerebellar syndrome
- Corneal dystrophy-perceptive deafness syndrome
- Crandall syndrome
- Cross syndrome
- DeSanctis–Cacchione syndrome
- De Barsy syndrome
- Dermatoosteolysis, Kirghizian type
- Donnai–Barrow syndrome
- Dubowitz syndrome
- Enamel-renal syndrome
- Familial nasal acilia
- Fertile eunuch syndrome
- Galactokinase deficiency
- Glucocorticoid deficiency 1
- Glutaminase deficiency
- Goldberg–Shprintzen syndrome
- Goldmann–Favre syndrome
- Gray platelet syndrome
- Hennekam syndrome
- Hydrolethalus syndrome
- Hypoprothrombinemia
- Immunodeficiency–centromeric instability–facial anomalies syndrome
- Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
- Infantile systemic hyalinosis
- Intellectual disability-spasticity-ectrodactyly syndrome
- Isolated 17,20-lyase deficiency
- Joubert syndrome
- Juvenile hyaline fibromatosis
- Kowarski syndrome
- Krabbe disease
- Kufor–Rakeb syndrome
- LPS-responsive beige-like anchor protein deficiency
- Lelis syndrome
- Letterer–Siwe disease
- Limb-girdle muscular dystrophy
- Lipoprotein lipase deficiency
- Lyngstadaas syndrome
- Majewski's polydactyly syndrome
- Malonyl-CoA decarboxylase deficiency
- McKusick–Kaufman syndrome
- Michels syndrome
- Miller syndrome
- Mismatch repair cancer syndrome
- Muscle–eye–brain disease
- Nakajo syndrome
- Odontoonychodermal dysplasia
- Oguchi disease
- Osteopetrosis
- Pyknoachondrogenesis
- Raine syndrome
- Renal dysplasia-limb defects syndrome
- Rotor syndrome
- Rudiger syndrome
- SLC35A1-CDG
- SOFT syndrome
- Saal Greenstein syndrome
- Sandhoff disease
- Schneckenbecken dysplasia
- Schwartz–Jampel syndrome
- Scott syndrome
- Sengers syndrome
- Senior–Løken syndrome
- Severe congenital neutropenia
- Short-limb skeletal dysplasia with severe combined immunodeficiency
- Sonoda syndrome
- Spondylo-meta-epiphyseal dysplasia
- Stimmler syndrome
- Succinyl-CoA:3-oxoacid CoA transferase deficiency
- TRIANGLE disease
- Trichothiodystrophy
- Turcot syndrome
- UV-sensitive syndrome
- Urban–Rogers–Meyer syndrome
- Vici syndrome
- Woodhouse–Sakati syndrome
- Woolly hair autosomal recessive