Inferior vermis hypoplasia
Symptom Information:
Symptom ID: | HPO:0007068 | ||
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HPO:
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Database Frequency: | 6 / 7739 | ||
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All diseases associated with this symptom:
Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome | (Orphanet:363429) |
Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency | (Orphanet:324262) |
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | (Orphanet:1369) |
Marden-Walker syndrome | (Orphanet:2461) |
Microphthalmia with brain and digit anomalies | (Orphanet:139471) |
X-linked complicated corpus callosum dysgenesis | (Orphanet:1497) |