Holoprosencephaly

MONDO:0016296

Holoprosencephaly (HPE) is a complex brain malformation resulting from incomplete cleavage of the prosencephalon, occurring between the 18th and 28th day of gestation, and affecting both the forebrain and face, which results in neurological manifestations and facial anomalies of variable severity.

Also known as: HPE, holoprosencephaly sequence

0 clinical trials for this condition and its sub-types, 0 tagged with Holoprosencephaly itself.

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Where it sits in the disease tree

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Part of

↑ Syndromic disease (7133) ↑ Hereditary neurological disease (5772) ↑ Congenital nervous system disorder (284) ↑ Multiple congenital anomalies/dysmorphic syndrome-intellectual disability (59) ↑ Non-acquired combined pituitary hormone deficiency (3)

Sub-types of Holoprosencephaly

Alobar holoprosencephaly 0 trials
2 sub-types
- Holoprosencephaly 5 0 trials
- Holoprosencephaly 9 0 trials
Chromosome 1q41-q42 deletion syndrome 0 trials
Holoprosencephaly 1 0 trials
Holoprosencephaly 10 0 trials
Holoprosencephaly 11 0 trials
Holoprosencephaly 12 with or without pancreatic agenesis 0 trials
Holoprosencephaly 13, X-linked 0 trials
Holoprosencephaly 14 0 trials
Holoprosencephaly 2 0 trials
Holoprosencephaly 3 0 trials
1 sub-type
- Solitary median maxillary central incisor syndrome 0 trials
Holoprosencephaly 4 0 trials
Holoprosencephaly 6 0 trials
Holoprosencephaly 7 0 trials
Holoprosencephaly 8 0 trials
Lobar holoprosencephaly 0 trials
2 sub-types
- Holoprosencephaly 5 0 trials
- Holoprosencephaly 9 0 trials
Microform holoprosencephaly 0 trials
3 sub-types
- Holoprosencephaly 5 0 trials
- Holoprosencephaly 9 0 trials
- Solitary median maxillary central incisor syndrome 0 trials
Semilobar holoprosencephaly 0 trials

Including sub-types (0) Tagged with Holoprosencephaly (0)

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