Greenberg dysplasia

MONDO:0008974

A very rare lethal skeletal dysplasia characterized by fetal hydrops, short limbs and abnormal chondro-osseous calcification. The disease is characterized by early in utero lethality and affected fetuses are considered as nonviable.

Also known as: Greenberg dysplasia, hem dysplasia, hydrops-ectopic calcification-motheaten syndrome, skeletal dysplasia, Greenberg type, GRBGD, Greenberg skeletal dysplasia, autosomal recessive lethal chondrodystrophy with congenital hydrops, chondrodystrophy, hydropic and prenatally lethal type

3 clinical trials for this condition and its sub-types.

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Broader categories

Disease (680) Metabolic disease (233) Musculoskeletal system disorder (207) Inherited lipid metabolism disorder (189) Hereditary disease (176) Bone disorder (51) Inborn errors of metabolism (45) Human disease (14) Developmental defect during embryogenesis (8) Skeletal system disorder (4)

Trials to join now! 2 Terminated 1

Scientists dive into rare cholesterol disorders to uncover clues

Knowledge-focused Terminated

This study looks at rare genetic disorders where the body can't make cholesterol properly, which can cause birth defects and learning problems. Researchers collect blood, urine, and tissue samples from affected people and their families to learn more about these conditions. The g…

Sponsor: Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) • Aim: Knowledge-focused

Last updated Aug 14, 2026 00:00 UTC

Greenberg dysplasia

Broader categories

Scientists dive into rare cholesterol disorders to uncover clues