Microcephaly 9, Primary, Autosomal Recessive (MCPH9)

Alias:
Mcph9
Primary Autosomal Recessive Microcephaly 9
Microcephaly, Type 9, Primary, Autosomal Recessive
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Microcephaly 9, Primary, Autosomal Recessive, also known as mcph9, is related to isolated growth hormone deficiency and female-restricted syndromic x-linked intellectual disability 99. An important gene associated with Microcephaly 9, Primary, Autosomal Recessive is CEP152 (Centrosomal Protein 152), and among its related pathways/superpathways are Cell Cycle, Mitotic and Loss of Nlp from mitotic centrosomes. Affiliated tissues include cortex and brain, and related phenotypes are self-injurious behavior and microcephaly
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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12
71
5

Medical Symptom

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

Gene & Mutation

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Disease Model

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MGI
Related Gene
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Publications
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References Literature

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