Van Maldergem syndrome
Human disease
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Van Maldergem syndrome
Summary
Van Maldergem syndrome is a developmental defect during embryogenesis[1].
Key Facts
- Van Maldergem syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- Van Maldergem syndrome's instance of is recorded as rare disease[3].
- Van Maldergem syndrome's instance of is recorded as class of disease[4].
- Van Maldergem syndrome is a type of syndrome[5].
- Van Maldergem syndrome is a type of Pashayan syndrome[6].
- Van Maldergem syndrome is a type of autosomal recessive disease[7].
- Van Maldergem syndrome's genetic association is recorded as FAT4[8].
- Van Maldergem syndrome's genetic association is recorded as DCHS1[9].
- Van Maldergem syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060238[10].
- Van Maldergem syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060238[11].
- Van Maldergem syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_314679[12].
- Van Maldergem syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].