MCID: WRM002
MIFTS: 6

Warman Mulliken Hayward Syndrome

Categories: Rare diseases

Aliases & Classifications for Warman Mulliken Hayward Syndrome

MalaCards integrated aliases for Warman Mulliken Hayward Syndrome:

Name: Warman Mulliken Hayward Syndrome 49 69
Craniosynostosis Boston Type 49
Craniosynostosis Warman Type 49

Classifications:



External Ids:

UMLS 69 C2931287

Summaries for Warman Mulliken Hayward Syndrome

NIH Rare Diseases : 49 The following summary is from Orphanet, a European reference portal for information on rare diseases and orphan drugs.Orpha Number: 1541Disease definitionCraniosynostosis, Boston type is a form of syndromic craniosynostosis (see this term), characterized by a highly variable craniosynostosis with frontal bossing, turribrachycephaly and cloverleaf skull anomaly. Hypoplasia of the supraorbital ridges, cleft palate, extra teeth and limb anomalies (triphalangeal thumb, 3-4 syndactyly of the hands, a short first metatarsal, middle phalangeal agenesis in the feet) have also been described. Associated problems include headache, poor vision, and seizures. Intelligence is normal.Visit the Orphanet disease page for more resources. Last updated: 7/9/2015

MalaCards based summary : Warman Mulliken Hayward Syndrome, also known as craniosynostosis boston type, is related to craniosynostosis 2.

Related Diseases for Warman Mulliken Hayward Syndrome

Diseases related to Warman Mulliken Hayward Syndrome via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 craniosynostosis 2 11.7

Symptoms & Phenotypes for Warman Mulliken Hayward Syndrome

Drugs & Therapeutics for Warman Mulliken Hayward Syndrome

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Anatomical Context for Warman Mulliken Hayward Syndrome

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Variations for Warman Mulliken Hayward Syndrome

Expression for Warman Mulliken Hayward Syndrome

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Pathways for Warman Mulliken Hayward Syndrome

GO Terms for Warman Mulliken Hayward Syndrome

Sources for Warman Mulliken Hayward Syndrome

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65 SNOMED-CT via HPO
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67 TGDB
68 Tocris
69 UMLS
70 UMLS via Orphanet
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