Holoprosencephaly 8
MONDO:0012267A holoprosencephaly that has material basis in variation in the chromosome region 14q13.
Also known as: HPE8, holoprosencephaly 8, holoprosencephaly type 8
0 clinical trials for this condition and its sub-types.
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Disease
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Nervous system disorder
(231)
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
(2)
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