FG syndrome type 1
ORPHA:93932Griscelli syndrome type 1
ORPHA:79476Griscelli syndrome type 2
ORPHA:79477Griscelli syndrome type 3
ORPHA:79478Heart-hand syndrome type 2
ORPHA:1350Heart-hand syndrome type 3
ORPHA:1342Hermansky-Pudlak syndrome due to AP3B1 deficiency
ORPHA:664500Holt-Oram syndrome
ORPHA:392Hyper-IgM syndrome type 2
ORPHA:101089Hyper-IgM syndrome type 3
ORPHA:101090Hyper-IgM syndrome type 4
ORPHA:101091Hyper-IgM syndrome type 5
ORPHA:101092IBIDS syndrome
ORPHA:453Immunodeficiency by defective expression of MHC class II
ORPHA:572Isolated Joubert syndrome
ORPHA:475Leukocyte adhesion deficiency type II
ORPHA:99843Macrocephaly-congenital heart disease-facial dysmorphism-intellectual disability syndrome
ORPHA:662175Malan overgrowth syndrome
ORPHA:420179Marfan syndrome type 1
ORPHA:284963Marfan syndrome type 2
ORPHA:284973Marfanoid syndrome, De Silva type
ORPHA:2464Mayer-Rokitansky-Küster-Hauser syndrome type 1
ORPHA:247775Mayer-Rokitansky-Küster-Hauser syndrome type 2
ORPHA:2578MGAT2-CDG
ORPHA:79329Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome
ORPHA:457284Microcephaly-microcornea syndrome, Seemanova type
ORPHA:2528MOGS-CDG
ORPHA:79330Monosomy 18p syndrome
ORPHA:1598Monosomy 18q syndrome
ORPHA:1600MPDU1-CDG
ORPHA:79323MPI-CDG
ORPHA:79319Mucopolysaccharidosis type 2, attenuated form
ORPHA:217093Mucopolysaccharidosis type 2, severe form
ORPHA:217085NPHP3-related Meckel-like syndrome
ORPHA:3032Orofaciodigital syndrome type 2
ORPHA:2751Otopalatodigital syndrome type 2
ORPHA:90652Peeling skin syndrome type A
ORPHA:263548Peeling skin syndrome type B
ORPHA:263553Perrault syndrome type 1
ORPHA:642945Perrault syndrome type 2
ORPHA:642976Pfeiffer syndrome type 1
ORPHA:93258Pfeiffer syndrome type 2
ORPHA:93259Pfeiffer syndrome type 3
ORPHA:93260PGM1-CDG
ORPHA:319646PHACE syndrome
ORPHA:42775PMM2-CDG
ORPHA:79318Port-wine nevi-mega cisterna magna-hydrocephalus syndrome
ORPHA:2703Progeroid syndrome, Petty type
ORPHA:2963