Holoprosencephaly 6
MONDO:0011616A holoprosencephaly that has material basis in variation in the chromosome region 2q37.1-q37.3.
Also known as: HPE6, holoprosencephaly 6, holoprosencephaly type 6
0 clinical trials for this condition and its sub-types.
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Disease
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Nervous system disorder
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Hereditary disease
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Endocrine system disorder
(72)
Syndromic disease
(25)
Hereditary endocrine growth disease
(24)
Human disease
(14)
Developmental defect during embryogenesis
(8)
Hereditary neurological disease
(6)
Disease of genetic or genomic mechanism
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