Clinical and research tests for Hunteria myriantha - Genetic Testing Registry (GTR)

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Results: 1 to 12 of 12

Select all conditions on this page	Conditions	Synonyms
Select item 7734	Mucopolysaccharidosis, MPS-II	Attenuated MPS (subtype; formerly known as mild MPS II) Hunter Syndrome I2S deficiency IDS deficiency Iduronate 2-sulfatase deficiency MPS 2 Mucopolysaccharidosis type 2 Mucopolysaccharidosis type II Mucopolysaccharidosis with skin involvement SIDS deficiency Severe MPS II Sulfoiduronate sulfatase deficiency
Select item 895748	Osteofibrous dysplasia	Tibia, bowing of, with pseudarthrosis and pectus excavatum
Select item 374138	Trigonocephaly-short stature-developmental delay syndrome	Hunter Rudd Hoffmann syndrome Say Meyer syndrome Trigonocephaly with short stature and developmental delay Trigonocephaly, short stature and developmental delay Trigonocephaly, short stature, and retarded psychomotor development
Select item 82852	Infantile neuroaxonal dystrophy	Infantile neuroaxonal dystrophy 1 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A Seitelberger disease
Select item 419681	Acromesomelic dysplasia 2C, Hunter-Thompson type	Acromesomelic dwarfism Acromesomelic dysplasia, Hunter-Thompson type
Select item 321949	Hunter-McAlpine craniosynostosis	Craniosynostosis, mental deficiency, almond-shaped palpebral fissures, downturned mouth, mild acral-skeletal anomalies, and short stature Hunter-McAlpine syndrome Hunter-mcalpine craniosynostosis syndrome
Select item 383181	Hunter-Macdonald syndrome
Select item 340516	Oculorenocerebellar syndrome	Absence of the cerebellar granular layer, mental retardation, tapetoretinal degeneration and progressive glomerulopathy ORC syndrome
Select item 930637	Trigonocephaly-broad thumbs syndrome
Select item 1814437	Night blindness-skeletal anomalies-dysmorphism syndrome
Select item 575246	Mucopolysaccharidosis type 2, severe form	Mucopolysaccharidosis, type II, severe form
Select item 1826165	Mucopolysaccharidosis type 2, attenuated form

Results: 1 to 12 of 12

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