OBSOLETE: Central polydactyly of toes
ORPHA:295010OBSOLETE: Central polydactyly of toes, bilateral
ORPHA:295185OBSOLETE: Central polydactyly of toes, unilateral
ORPHA:295183OBSOLETE: Adactyly of foot
ORPHA:435623OBSOLETE: Benign exophthalmos syndrome
ORPHA:71269OBSOLETE: Central polydactyly of fingers, bilateral
ORPHA:295173OBSOLETE: Central polydactyly of fingers, unilateral
ORPHA:295171OBSOLETE: Familial hyperreninemic hypoaldosteronism type 1
ORPHA:99763OBSOLETE: Familial hyperreninemic hypoaldosteronism type 2
ORPHA:99764OBSOLETE: Fibrocalculous pancreatopathy
ORPHA:99654OBSOLETE: Microcephaly-seizures-developmental delay syndrome
ORPHA:228418OBSOLETE: Multicentric Castleman disease
ORPHA:93686OBSOLETE: Split foot
ORPHA:294994OBSOLETE: Split foot, bilateral
ORPHA:295126OBSOLETE: Split foot, unilateral
ORPHA:295124OBSOLETE: Xeroderma pigmentosum complementation group A
ORPHA:276249OBSOLETE: Xeroderma pigmentosum complementation group B
ORPHA:276252OBSOLETE: Xeroderma pigmentosum complementation group C
ORPHA:276255OBSOLETE: Xeroderma pigmentosum complementation group D
ORPHA:276258OBSOLETE: Xeroderma pigmentosum complementation group E
ORPHA:276261OBSOLETE: Xeroderma pigmentosum complementation group F
ORPHA:276264OBSOLETE: Xeroderma pigmentosum complementation group G
ORPHA:276267