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(Q47455810)
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growth hormone insensitivity syndrome
group of hereditary diseases
GHIS
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Statements
instance of
class of disease
0 references
subclass of
dwarfism
0 references
rare genetic hypothalamic or pituitary disease
0 references
NCI Thesaurus ID
C129867
0 references
has part(s)
Laron syndrome
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acid-labile subunit deficiency
0 references
Laron syndrome with immunodeficiency
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growth delay due to insulin-like growth factor type 1 deficiency
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growth delay due to insulin-like growth factor I resistance
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short stature due to partial GHR deficiency
0 references
Identifiers
ICD-11 (foundation)
510125881
0 references
Orphanet ID
181393
0 references
UMLS CUI
C0271568
0 references
C4318479
1 reference
based on heuristic
inferred by common Orphanet mappings on source and on Wikidata
stated in
UMLS 2023
retrieved
16 June 2023
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