Isolated Growth Hormone Deficiency, Type Ib (IGHD1B)

Alias:
Isolated Growth Hormone Deficiency Type Ib
Congenital Isolated Growth Hormone Deficiency Type Ib
Growth Hormone Deficiency, Isolated, Type Ib
Congenital Isolated Gh Deficiency Type Ib
Congenital Ighd Type Ib
Ighd Ib
Pituitary Dwarfism I
Ighd1b
Growth Hormone Deficiency, Isolated, 1b
Dwarfism of Sindh
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Isolated Growth Hormone Deficiency, Type Ib, also known as isolated growth hormone deficiency type ib, is related to isolated growth hormone deficiency and isolated growth hormone deficiency, type ia. An important gene associated with Isolated Growth Hormone Deficiency, Type Ib is GH1 (Growth Hormone 1), and among its related pathways/superpathways are Signal Transduction and GPCR downstream signalling. The drug Hormones has been mentioned in the context of this disorder. Affiliated tissues include pituitary and bone, and related phenotypes are short stature and micropenis
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Newborn
--
20
144
7

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Mutations
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Related Drugs

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No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
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References Literature

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IF
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